Structured Review

Cell Signaling Technology Inc na k atpase
Effect of garlic and its metabolites on Na + /K + <t>-ATPase</t> expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p
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Images

1) Product Images from "Novel Sulfur Metabolites of Garlic Attenuate Cardiac Hypertrophy and Remodeling through Induction of Na+/K+-ATPase Expression"

Article Title: Novel Sulfur Metabolites of Garlic Attenuate Cardiac Hypertrophy and Remodeling through Induction of Na+/K+-ATPase Expression

Journal: Frontiers in Pharmacology

doi: 10.3389/fphar.2017.00018

Effect of garlic and its metabolites on Na + /K + -ATPase expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p
Figure Legend Snippet: Effect of garlic and its metabolites on Na + /K + -ATPase expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p

Techniques Used: Expressing, Western Blot

2) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

3) Product Images from "Cellular Asymmetric Catalysis by UDP-glucuronosyltransferase 1A8 Shows Functional Localization to the Basolateral Plasma Membrane *"

Article Title: Cellular Asymmetric Catalysis by UDP-glucuronosyltransferase 1A8 Shows Functional Localization to the Basolateral Plasma Membrane *

Journal: The Journal of Biological Chemistry

doi: 10.1074/jbc.M114.634428

Cell surface biotinylation of HT29-MTX cells. A, specificity of antibodies used for UGT1A and control protein detection with the ProteinSimple SIMON system. B, relative peak area of protein levels detected in surface biotinylation samples after streptavidin pulldown (UGT1A, Na + /K + -ATPase) and in whole cell lysate (GAPDH).
Figure Legend Snippet: Cell surface biotinylation of HT29-MTX cells. A, specificity of antibodies used for UGT1A and control protein detection with the ProteinSimple SIMON system. B, relative peak area of protein levels detected in surface biotinylation samples after streptavidin pulldown (UGT1A, Na + /K + -ATPase) and in whole cell lysate (GAPDH).

Techniques Used:

4) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

5) Product Images from "Insulin regulates GLUT4 in the ventromedial hypothalamus to restore the sympathoadrenal response to hypoglycemia in diabetic rats"

Article Title: Insulin regulates GLUT4 in the ventromedial hypothalamus to restore the sympathoadrenal response to hypoglycemia in diabetic rats

Journal: American Journal of Physiology - Endocrinology and Metabolism

doi: 10.1152/ajpendo.00324.2018

A–E : phosphorylation of Akt and protein levels of total and plasma membrane (PM) glucose transporters (GLUT4 and GLUT3) in the ventromedial hypothalamus (VMH) of nondiabetic control (CON) and streptozotocin-diabetic (DIAB) rats in the basal state (i.e., not subjected to hyperinsulinemic clamp) and during acute intravenous infusion of insulin during hyperinsulinemic clamp. Nondiabetic control rats had been infused chronically (i.e., for 2 wk) with artificial cerebrospinal fluid (aCSF) into the VMH (CON/VMHaCSF); diabetic rats had been infused chronically with aCSF (DIAB/VMHaCSF) or regular insulin (DIAB/VMH-Ins) into the VMH. Actin and Na-K-ATPase proteins were used as internal control to normalize data for total and PM GLUT levels, respectively. F : correlation analysis of total GLUT4 with peak epinephrine levels in nondiabetic controls (CON/VMHaCSF) and diabetic rats (DIAB/VMHaCSF and DIAB/VMH-Ins). GLUT4 content is expressed relative to control rat GLUT4 content during the basal state (CON/VMHaCSF). Values are means ± SE ( n = 8/group). * P
Figure Legend Snippet: A–E : phosphorylation of Akt and protein levels of total and plasma membrane (PM) glucose transporters (GLUT4 and GLUT3) in the ventromedial hypothalamus (VMH) of nondiabetic control (CON) and streptozotocin-diabetic (DIAB) rats in the basal state (i.e., not subjected to hyperinsulinemic clamp) and during acute intravenous infusion of insulin during hyperinsulinemic clamp. Nondiabetic control rats had been infused chronically (i.e., for 2 wk) with artificial cerebrospinal fluid (aCSF) into the VMH (CON/VMHaCSF); diabetic rats had been infused chronically with aCSF (DIAB/VMHaCSF) or regular insulin (DIAB/VMH-Ins) into the VMH. Actin and Na-K-ATPase proteins were used as internal control to normalize data for total and PM GLUT levels, respectively. F : correlation analysis of total GLUT4 with peak epinephrine levels in nondiabetic controls (CON/VMHaCSF) and diabetic rats (DIAB/VMHaCSF and DIAB/VMH-Ins). GLUT4 content is expressed relative to control rat GLUT4 content during the basal state (CON/VMHaCSF). Values are means ± SE ( n = 8/group). * P

Techniques Used:

6) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

7) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

8) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

9) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

10) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

11) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

12) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

13) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

14) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

15) Product Images from "Macrophage SR-BI mediates efferocytosis via Src/PI3K/Rac1 signaling and reduces atherosclerotic lesion necrosis [S]"

Article Title: Macrophage SR-BI mediates efferocytosis via Src/PI3K/Rac1 signaling and reduces atherosclerotic lesion necrosis [S]

Journal: Journal of Lipid Research

doi: 10.1194/jlr.M056689

SR-BI interacts with Src in macrophages, inducing Src phosphorylation and membrane recruitment of Src. A: WT macrophage cell lysates were immunoprecipitated with either anti-SR-BI or anti-LRP1 antibodies and protein A/G magnetic beads. Immunoprecipitated GULP or SR-BI as a control was then detected by Western blotting. B: WT macrophage cell lysates were immunoprecipitated with either anti-SR-BI or anti-Src antibodies and protein A/G magnetic beads. Immunoprecipitated Src or SR-BI was then detected by Western blotting. C: SR-BI plasmid was transfected for the indicated times into WT or SR-BI −/− macrophages using Lipofectamine LTX and Plus reagent. Plasma membrane proteins were isolated as described in the Materials and Methods and the SR-BI, pSrc (Tyr 416), and Na + /K + ATPase levels were detected by Western blotting. D: Efferocytosis was measured by flow cytometry from WT and SR-BI −/− macrophages transfected with pCMV6-mSR-BI plasmid or sham as described in the Materials and Methods. A–C: Data are representative of three experiments.
Figure Legend Snippet: SR-BI interacts with Src in macrophages, inducing Src phosphorylation and membrane recruitment of Src. A: WT macrophage cell lysates were immunoprecipitated with either anti-SR-BI or anti-LRP1 antibodies and protein A/G magnetic beads. Immunoprecipitated GULP or SR-BI as a control was then detected by Western blotting. B: WT macrophage cell lysates were immunoprecipitated with either anti-SR-BI or anti-Src antibodies and protein A/G magnetic beads. Immunoprecipitated Src or SR-BI was then detected by Western blotting. C: SR-BI plasmid was transfected for the indicated times into WT or SR-BI −/− macrophages using Lipofectamine LTX and Plus reagent. Plasma membrane proteins were isolated as described in the Materials and Methods and the SR-BI, pSrc (Tyr 416), and Na + /K + ATPase levels were detected by Western blotting. D: Efferocytosis was measured by flow cytometry from WT and SR-BI −/− macrophages transfected with pCMV6-mSR-BI plasmid or sham as described in the Materials and Methods. A–C: Data are representative of three experiments.

Techniques Used: Immunoprecipitation, Magnetic Beads, Western Blot, Plasmid Preparation, Transfection, Isolation, Flow Cytometry, Cytometry

16) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

17) Product Images from "Novel Sulfur Metabolites of Garlic Attenuate Cardiac Hypertrophy and Remodeling through Induction of Na+/K+-ATPase Expression"

Article Title: Novel Sulfur Metabolites of Garlic Attenuate Cardiac Hypertrophy and Remodeling through Induction of Na+/K+-ATPase Expression

Journal: Frontiers in Pharmacology

doi: 10.3389/fphar.2017.00018

Effect of garlic and its metabolites on Na + /K + -ATPase expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p
Figure Legend Snippet: Effect of garlic and its metabolites on Na + /K + -ATPase expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p

Techniques Used: Expressing, Western Blot

18) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

19) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

20) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

21) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

22) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

23) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

24) Product Images from "Intracellular Calcium Regulates Nonsense-Mediated mRNA Decay"

Article Title: Intracellular Calcium Regulates Nonsense-Mediated mRNA Decay

Journal: Nature medicine

doi: 10.1038/nm.3620

Cardiac glycosides block NMD through inhibition of Na + /K + -ATPase and elevation of intracellular calcium ( a ) Ratios of CBR/CBG bioluminescence signals in mouse dermal fibroblasts (left panel) or human U2OS cells (right panel) expressing the NMD reporter after 24 h treatment with DMSO, caffeine, or various concentrations of ouabain. The ratio in DMSO-treated reporter cells was normalized to 1. Data represent the mean ± SD of three biological replicates. ( b ) Ratios of CBR/CBG bioluminescence signals in human U2OS reporter cells expressing either empty vector, rat α1 subunit or rat α3 subunit of Na + /K + -ATPase after 24 h treatment with DMSO or ouabain. The ratio in DMSO-treated reporter cells was normalized to 1. Data represent the mean ± SD of three independent experiments. * P
Figure Legend Snippet: Cardiac glycosides block NMD through inhibition of Na + /K + -ATPase and elevation of intracellular calcium ( a ) Ratios of CBR/CBG bioluminescence signals in mouse dermal fibroblasts (left panel) or human U2OS cells (right panel) expressing the NMD reporter after 24 h treatment with DMSO, caffeine, or various concentrations of ouabain. The ratio in DMSO-treated reporter cells was normalized to 1. Data represent the mean ± SD of three biological replicates. ( b ) Ratios of CBR/CBG bioluminescence signals in human U2OS reporter cells expressing either empty vector, rat α1 subunit or rat α3 subunit of Na + /K + -ATPase after 24 h treatment with DMSO or ouabain. The ratio in DMSO-treated reporter cells was normalized to 1. Data represent the mean ± SD of three independent experiments. * P

Techniques Used: Blocking Assay, Inhibition, Expressing, Plasmid Preparation

25) Product Images from "Growth differentiation factor-15 promotes glutamate release in medial prefrontal cortex of mice through upregulation of T-type calcium channels"

Article Title: Growth differentiation factor-15 promotes glutamate release in medial prefrontal cortex of mice through upregulation of T-type calcium channels

Journal: Scientific Reports

doi: 10.1038/srep28653

GDF-15 enhanced Ca V 3.1 and Ca V 3.3 surface expression on pyramidal neurons in mPFC. ( A ) Microscopic confocal images showing expression of Ca V 3.1, Ca V 3.2 and Ca V 3.3 α-subunits of T-type VGCCs on pyramidal neurons in mPFC. Bar = 50 μm. ( B ) Western blot showing effects of GDF-15 on T-type VGCC surface expression. Na + /K + -ATPase was used as loading control. ( C , D ) Western blot showing effects of LY2109761, SB431542, and U0126 on GDF-15-induced enhancement of Ca V 3.1 and Ca V 3.3 surface expression. Results are shown as means ± SEM. * p
Figure Legend Snippet: GDF-15 enhanced Ca V 3.1 and Ca V 3.3 surface expression on pyramidal neurons in mPFC. ( A ) Microscopic confocal images showing expression of Ca V 3.1, Ca V 3.2 and Ca V 3.3 α-subunits of T-type VGCCs on pyramidal neurons in mPFC. Bar = 50 μm. ( B ) Western blot showing effects of GDF-15 on T-type VGCC surface expression. Na + /K + -ATPase was used as loading control. ( C , D ) Western blot showing effects of LY2109761, SB431542, and U0126 on GDF-15-induced enhancement of Ca V 3.1 and Ca V 3.3 surface expression. Results are shown as means ± SEM. * p

Techniques Used: Expressing, Western Blot

26) Product Images from "Insulin regulates GLUT4 in the ventromedial hypothalamus to restore the sympathoadrenal response to hypoglycemia in diabetic rats"

Article Title: Insulin regulates GLUT4 in the ventromedial hypothalamus to restore the sympathoadrenal response to hypoglycemia in diabetic rats

Journal: American Journal of Physiology - Endocrinology and Metabolism

doi: 10.1152/ajpendo.00324.2018

A–E : phosphorylation of Akt and protein levels of total and plasma membrane (PM) glucose transporters (GLUT4 and GLUT3) in the ventromedial hypothalamus (VMH) of nondiabetic control (CON) and streptozotocin-diabetic (DIAB) rats in the basal state (i.e., not subjected to hyperinsulinemic clamp) and during acute intravenous infusion of insulin during hyperinsulinemic clamp. Nondiabetic control rats had been infused chronically (i.e., for 2 wk) with artificial cerebrospinal fluid (aCSF) into the VMH (CON/VMHaCSF); diabetic rats had been infused chronically with aCSF (DIAB/VMHaCSF) or regular insulin (DIAB/VMH-Ins) into the VMH. Actin and Na-K-ATPase proteins were used as internal control to normalize data for total and PM GLUT levels, respectively. F : correlation analysis of total GLUT4 with peak epinephrine levels in nondiabetic controls (CON/VMHaCSF) and diabetic rats (DIAB/VMHaCSF and DIAB/VMH-Ins). GLUT4 content is expressed relative to control rat GLUT4 content during the basal state (CON/VMHaCSF). Values are means ± SE ( n = 8/group). * P
Figure Legend Snippet: A–E : phosphorylation of Akt and protein levels of total and plasma membrane (PM) glucose transporters (GLUT4 and GLUT3) in the ventromedial hypothalamus (VMH) of nondiabetic control (CON) and streptozotocin-diabetic (DIAB) rats in the basal state (i.e., not subjected to hyperinsulinemic clamp) and during acute intravenous infusion of insulin during hyperinsulinemic clamp. Nondiabetic control rats had been infused chronically (i.e., for 2 wk) with artificial cerebrospinal fluid (aCSF) into the VMH (CON/VMHaCSF); diabetic rats had been infused chronically with aCSF (DIAB/VMHaCSF) or regular insulin (DIAB/VMH-Ins) into the VMH. Actin and Na-K-ATPase proteins were used as internal control to normalize data for total and PM GLUT levels, respectively. F : correlation analysis of total GLUT4 with peak epinephrine levels in nondiabetic controls (CON/VMHaCSF) and diabetic rats (DIAB/VMHaCSF and DIAB/VMH-Ins). GLUT4 content is expressed relative to control rat GLUT4 content during the basal state (CON/VMHaCSF). Values are means ± SE ( n = 8/group). * P

Techniques Used:

27) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

28) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

29) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

30) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

31) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

32) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

33) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

34) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

35) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

36) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

37) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

38) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

39) Product Images from "Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development"

Article Title: Multiple roles for the Na,K-ATPase subunits, Atp1a1 and Fxyd1, during brain ventricle development

Journal: Developmental Biology

doi: 10.1016/j.ydbio.2012.05.034

The Na,K-ATPase is required for brain ventricle development
Figure Legend Snippet: The Na,K-ATPase is required for brain ventricle development

Techniques Used:

Na,K-ATPase pumping is required for brain ventricle development
Figure Legend Snippet: Na,K-ATPase pumping is required for brain ventricle development

Techniques Used:

Model for requirement of Na,K-ATPase during brain ventricle development
Figure Legend Snippet: Model for requirement of Na,K-ATPase during brain ventricle development

Techniques Used:

40) Product Images from "Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase"

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

Journal: The Biochemical journal

doi: 10.1042/BJ20111398

Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells
Figure Legend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

Techniques Used: Expressing, Mutagenesis

Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells
Figure Legend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

Techniques Used:

Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells
Figure Legend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

Techniques Used:

Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938
Figure Legend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

Techniques Used:

Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells
Figure Legend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

Techniques Used:

Related Articles

Incubation:

Article Title: Insulin regulates GLUT4 in the ventromedial hypothalamus to restore the sympathoadrenal response to hypoglycemia in diabetic rats
Article Snippet: .. Polyvinylidene difluoride (PVDF) membranes (Millipore) were incubated with the following primary antibodies: anti-phosphorylated Akt (1:1,000 dilution; Cell Signaling Technology, Danvers, MA), anti-Akt (1:1,000 dilution; Cell Signaling Technology), anti-GLUT3 (1:1,000; Santa Cruz Biotechnology, Santa Cruz, CA), anti-GLUT4 (1:1,000 dilution; Millipore), β-actin (1:1,000, Sigma-Aldrich, St. Louis, MO), and Na-K-ATPase (1:1,000 dilution; Cell Signaling Technology). .. After incubation with horseradish peroxidase-conjugated anti-rabbit (1:10,000; Cell Signaling Technology) or anti-mouse (1:10,000 dilution; Millipore) IgG secondary antibody, the immunocomplexes were visualized by chemiluminescence using Amersham ECL Western blot detection reagents (GE HeathCare Bio-Sciences, Piscataway, NJ) and quantified using ImageJ software.

other:

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase
Article Snippet: Under control conditions ~ 17 % of the Na+/ K+ -ATPase from α -1.S11A/S18A cells bound to digoxin-affinity columns was eluted by Solution #1 and therefore is in Population #1 ( and ).

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase
Article Snippet: Thus it is very likely that Ang II-dependent phosphorylation of rat kidney Na+/ K+ -ATPase can regulate the intrinsic properties of the Na+/ K+ -ATPase in the rat proximal tubule, and that more than one population of Na+/ K+ -ATPase in the plasma membrane is part of this regulatory mechanism.

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase
Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

Article Title: Novel Sulfur Metabolites of Garlic Attenuate Cardiac Hypertrophy and Remodeling through Induction of Na+/K+-ATPase Expression
Article Snippet: Garlic and Its Metabolites Failed to Show Any Anti-Hypertrophic Effect in H9C2 Cells in Presence of Na+ /K+ -ATPase Inhibitor To confirm whether garlic and its metabolites showed their anti-hypertrophic effect through Na+ /K+ -ATPase, we treated H9C2 cells with Iso in presence and absence of digoxin, a Na+ /K+ -ATPase inhibitor.

Article Title: Cellular Asymmetric Catalysis by UDP-glucuronosyltransferase 1A8 Shows Functional Localization to the Basolateral Plasma Membrane *
Article Snippet: UGT1A was obtained from Santa Cruz Biotechnology (Dallas, TX); GAPDH, Na+ /K+ -ATPase, and α-actinin were from Cell Signaling Technologies (New England Biolabs, Herts, UK).

Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase
Article Snippet: Anti-P-Ser18 antibody also detected another protein that was not the Na+/ K+ -ATPase that ran below the α -subunit ( , top panel, lanes 1–8).

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    Cell Signaling Technology Inc na k atpase
    Effect of garlic and its metabolites on Na + /K + <t>-ATPase</t> expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p
    Na K Atpase, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effect of garlic and its metabolites on Na + /K + -ATPase expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p

    Journal: Frontiers in Pharmacology

    Article Title: Novel Sulfur Metabolites of Garlic Attenuate Cardiac Hypertrophy and Remodeling through Induction of Na+/K+-ATPase Expression

    doi: 10.3389/fphar.2017.00018

    Figure Lengend Snippet: Effect of garlic and its metabolites on Na + /K + -ATPase expression. (A,B) Western blot and bar graph of Na + /K + -ATPase from H9C2 cells. (C,D) Western blot and bar graph of Na + /K + -ATPase from rat heart. (Gels and blots were cropped and run under same experimental conditions). ( N = 3). Data were shown as mean ± SEM, ∗ p

    Article Snippet: Garlic and Its Metabolites Failed to Show Any Anti-Hypertrophic Effect in H9C2 Cells in Presence of Na+ /K+ -ATPase Inhibitor To confirm whether garlic and its metabolites showed their anti-hypertrophic effect through Na+ /K+ -ATPase, we treated H9C2 cells with Iso in presence and absence of digoxin, a Na+ /K+ -ATPase inhibitor.

    Techniques: Expressing, Western Blot

    Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Stable expression of wild-type and mutant forms of rat α -1 subunit of Na+ /K+ -ATPase in OK cells

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques: Expressing, Mutagenesis

    Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Relative effect of Ang II on the elution of plasma membrane protein containing Populations #1, #2 and #3 of Na + /K + -ATPase from rat α -1.wild-type (A), α -1.S11A/S18A (B) and α -1.S938A (C) cells

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques:

    Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Three populations of Na+ /K+ -ATPase in plasma membranes of α -1.S11A/S18A and α -1.S938A cells

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques:

    Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 18

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques:

    Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 11

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques:

    Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Phosphorylation of rat kidney Na + /K + -ATPase at Ser 938

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques:

    Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

    Journal: The Biochemical journal

    Article Title: Angiotensin II-dependent phosphorylation at Ser11/Ser18 and Ser938 shifts the E2 conformations of rat kidney Na+/K+-ATPase

    doi: 10.1042/BJ20111398

    Figure Lengend Snippet: Elution from digoxin-affinity columns of plasma membrane protein containing Na + /K + -ATPase Populations #1 (fractions 1–9), #2 (fractions 10–18) and #3 (fractions 19–22) from control and Ang II-treated α -1.S11A/S18A cells

    Article Snippet: This is the first demonstration that Ang II-dependent phosphorylation of any form of Na+/ K+ -ATPase can regulate any of the basic biochemical properties of the Na+/ K+ -ATPase.

    Techniques:

    Cell surface biotinylation of HT29-MTX cells. A, specificity of antibodies used for UGT1A and control protein detection with the ProteinSimple SIMON system. B, relative peak area of protein levels detected in surface biotinylation samples after streptavidin pulldown (UGT1A, Na + /K + -ATPase) and in whole cell lysate (GAPDH).

    Journal: The Journal of Biological Chemistry

    Article Title: Cellular Asymmetric Catalysis by UDP-glucuronosyltransferase 1A8 Shows Functional Localization to the Basolateral Plasma Membrane *

    doi: 10.1074/jbc.M114.634428

    Figure Lengend Snippet: Cell surface biotinylation of HT29-MTX cells. A, specificity of antibodies used for UGT1A and control protein detection with the ProteinSimple SIMON system. B, relative peak area of protein levels detected in surface biotinylation samples after streptavidin pulldown (UGT1A, Na + /K + -ATPase) and in whole cell lysate (GAPDH).

    Article Snippet: UGT1A was obtained from Santa Cruz Biotechnology (Dallas, TX); GAPDH, Na+ /K+ -ATPase, and α-actinin were from Cell Signaling Technologies (New England Biolabs, Herts, UK).

    Techniques: