total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt
    Effects of ADAM12 on oncogenic signaling pathways in the human colorectal cancer cells. Representative western blot images and semi-quantification graphs for the phosphorylation levels of PDK1, GSK-3β and <t>AKT</t> in AV-transfected or AS-transfected DLD1 or SW480 cells. Data are presented as the mean ± SD (n=3). * P<0.05. ADAM12, a disintegrin and metalloprotease 12; PDK1, phosphoinositide-dependent protein kinase 1; <t>GSK-3β,</t> <t>glycogen</t> synthase kinase-3β; EV, empty pcDNA6-myc vector; AV, ADAM12-pcDNA6-myc construct; SS, scrambled siRNA; AS, ADAM12 siRNA; siRNA, small interfering RNA; p-, phosphorylated; T-, total.
    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "A disintegrin and metalloprotease 12 contributes to colorectal cancer metastasis by regulating epithelial-mesenchymal transition"

    Article Title: A disintegrin and metalloprotease 12 contributes to colorectal cancer metastasis by regulating epithelial-mesenchymal transition

    Journal: International Journal of Oncology

    doi: 10.3892/ijo.2023.5498

    Effects of ADAM12 on oncogenic signaling pathways in the human colorectal cancer cells. Representative western blot images and semi-quantification graphs for the phosphorylation levels of PDK1, GSK-3β and AKT in AV-transfected or AS-transfected DLD1 or SW480 cells. Data are presented as the mean ± SD (n=3). * P<0.05. ADAM12, a disintegrin and metalloprotease 12; PDK1, phosphoinositide-dependent protein kinase 1; GSK-3β, glycogen synthase kinase-3β; EV, empty pcDNA6-myc vector; AV, ADAM12-pcDNA6-myc construct; SS, scrambled siRNA; AS, ADAM12 siRNA; siRNA, small interfering RNA; p-, phosphorylated; T-, total.
    Figure Legend Snippet: Effects of ADAM12 on oncogenic signaling pathways in the human colorectal cancer cells. Representative western blot images and semi-quantification graphs for the phosphorylation levels of PDK1, GSK-3β and AKT in AV-transfected or AS-transfected DLD1 or SW480 cells. Data are presented as the mean ± SD (n=3). * P<0.05. ADAM12, a disintegrin and metalloprotease 12; PDK1, phosphoinositide-dependent protein kinase 1; GSK-3β, glycogen synthase kinase-3β; EV, empty pcDNA6-myc vector; AV, ADAM12-pcDNA6-myc construct; SS, scrambled siRNA; AS, ADAM12 siRNA; siRNA, small interfering RNA; p-, phosphorylated; T-, total.

    Techniques Used: Western Blot, Transfection, Plasmid Preparation, Construct, Small Interfering RNA

    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt
    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt
    List of Antibodies for Western Blotting and IHC
    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Hepatocyte Smoothened Activity Controls Susceptibility to Insulin Resistance and Nonalcoholic Fatty Liver Disease"

    Article Title: Hepatocyte Smoothened Activity Controls Susceptibility to Insulin Resistance and Nonalcoholic Fatty Liver Disease

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    doi: 10.1016/j.jcmgh.2022.12.008

    List of Antibodies for Western Blotting and IHC
    Figure Legend Snippet: List of Antibodies for Western Blotting and IHC

    Techniques Used: Western Blot

    anti total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti total akt
    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling <t>pathways</t> <t>ERK1/2,</t> <t>Akt</t> and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .
    Anti Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "2-Arachidonoylglycerol Modulates CXCL12-Mediated Chemotaxis in Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia"

    Article Title: 2-Arachidonoylglycerol Modulates CXCL12-Mediated Chemotaxis in Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia

    Journal: Cancers

    doi: 10.3390/cancers15051585

    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, Akt and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .
    Figure Legend Snippet: Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, Akt and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .

    Techniques Used: Activation Assay, Incubation, Western Blot

    Effects of inhibiting the cannabinoid receptors on Akt and p38 activation. JeKo-1 cells were treated for 20 min with the CB1 antagonist SR141716 (10 nM), or with the CB2 inverse agonist SR1445282 (10 nM), prior to be incubated for 2 min with 2-AG. Activation of the signaling pathways ( A ) Akt and ( B ) p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of three repeats and error bars are standard error of the mean; 2-AG condition is shown as normalized to incubation with vehicle set as 1, unpaired t -test with Welch’s correction, # p < 0.05.
    Figure Legend Snippet: Effects of inhibiting the cannabinoid receptors on Akt and p38 activation. JeKo-1 cells were treated for 20 min with the CB1 antagonist SR141716 (10 nM), or with the CB2 inverse agonist SR1445282 (10 nM), prior to be incubated for 2 min with 2-AG. Activation of the signaling pathways ( A ) Akt and ( B ) p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of three repeats and error bars are standard error of the mean; 2-AG condition is shown as normalized to incubation with vehicle set as 1, unpaired t -test with Welch’s correction, # p < 0.05.

    Techniques Used: Activation Assay, Incubation, Western Blot

    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt
    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, <t>Akt</t> <t>and</t> <t>p38</t> was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .
    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total akt/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    86/100 stars

    Images

    1) Product Images from "2-Arachidonoylglycerol Modulates CXCL12-Mediated Chemotaxis in Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia"

    Article Title: 2-Arachidonoylglycerol Modulates CXCL12-Mediated Chemotaxis in Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia

    Journal: Cancers

    doi: 10.3390/cancers15051585

    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, Akt and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .
    Figure Legend Snippet: Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, Akt and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .

    Techniques Used: Activation Assay, Incubation, Western Blot

    Effects of inhibiting the cannabinoid receptors on Akt and p38 activation. JeKo-1 cells were treated for 20 min with the CB1 antagonist SR141716 (10 nM), or with the CB2 inverse agonist SR1445282 (10 nM), prior to be incubated for 2 min with 2-AG. Activation of the signaling pathways ( A ) Akt and ( B ) p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of three repeats and error bars are standard error of the mean; 2-AG condition is shown as normalized to incubation with vehicle set as 1, unpaired t -test with Welch’s correction, # p < 0.05.
    Figure Legend Snippet: Effects of inhibiting the cannabinoid receptors on Akt and p38 activation. JeKo-1 cells were treated for 20 min with the CB1 antagonist SR141716 (10 nM), or with the CB2 inverse agonist SR1445282 (10 nM), prior to be incubated for 2 min with 2-AG. Activation of the signaling pathways ( A ) Akt and ( B ) p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of three repeats and error bars are standard error of the mean; 2-AG condition is shown as normalized to incubation with vehicle set as 1, unpaired t -test with Welch’s correction, # p < 0.05.

    Techniques Used: Activation Assay, Incubation, Western Blot

    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt
    <t>HG-induced</t> <t>TSP1</t> upregulation requires <t>PI3K/Akt.</t> HG (48 h)-induced TSP1 upregulation in MC was attenuated by the PI3K inhibitors (A) LY294002 and (B) wortmannin as well as (C) Akt inhibitor VIII ( n = 10, ** p < 0.01, *** p < 0.005). (D) TSP1 transcript upregulation by HG (24 h) was inhibited by Akt inhibitor VIII ( n = 4, * p < 0.05). HG (48 h)-induced TSP1 promoter activity, assessed using a luciferase reporter construct, was also inhibited by (E) LY294002 ( n = 3, * p < 0.05, ** p < 0.01, *** p < 0.005, **** p < 0.0001), (F) wortmannin ( n = 9, * p < 0.05, ** p < 0.01, **** p < 0.001), or (G) Akt inhibitor VIII ( n = 9, **** p < 0.001) in MC.
    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Cell surface GRP78 regulates TGFβ1-mediated profibrotic responses via TSP1 in diabetic kidney disease"

    Article Title: Cell surface GRP78 regulates TGFβ1-mediated profibrotic responses via TSP1 in diabetic kidney disease

    Journal: Frontiers in Pharmacology

    doi: 10.3389/fphar.2023.1098321

    HG-induced TSP1 upregulation requires PI3K/Akt. HG (48 h)-induced TSP1 upregulation in MC was attenuated by the PI3K inhibitors (A) LY294002 and (B) wortmannin as well as (C) Akt inhibitor VIII ( n = 10, ** p < 0.01, *** p < 0.005). (D) TSP1 transcript upregulation by HG (24 h) was inhibited by Akt inhibitor VIII ( n = 4, * p < 0.05). HG (48 h)-induced TSP1 promoter activity, assessed using a luciferase reporter construct, was also inhibited by (E) LY294002 ( n = 3, * p < 0.05, ** p < 0.01, *** p < 0.005, **** p < 0.0001), (F) wortmannin ( n = 9, * p < 0.05, ** p < 0.01, **** p < 0.001), or (G) Akt inhibitor VIII ( n = 9, **** p < 0.001) in MC.
    Figure Legend Snippet: HG-induced TSP1 upregulation requires PI3K/Akt. HG (48 h)-induced TSP1 upregulation in MC was attenuated by the PI3K inhibitors (A) LY294002 and (B) wortmannin as well as (C) Akt inhibitor VIII ( n = 10, ** p < 0.01, *** p < 0.005). (D) TSP1 transcript upregulation by HG (24 h) was inhibited by Akt inhibitor VIII ( n = 4, * p < 0.05). HG (48 h)-induced TSP1 promoter activity, assessed using a luciferase reporter construct, was also inhibited by (E) LY294002 ( n = 3, * p < 0.05, ** p < 0.01, *** p < 0.005, **** p < 0.0001), (F) wortmannin ( n = 9, * p < 0.05, ** p < 0.01, **** p < 0.001), or (G) Akt inhibitor VIII ( n = 9, **** p < 0.001) in MC.

    Techniques Used: Activity Assay, Luciferase, Construct

    HG-induced TGFβ1 activation and signaling are blocked by PI3K/Akt inhibition. HG (48 h)-induced TGFβ1 activation, assessed by ELISA of medium without acid activation, was prevented by PI3K inhibition using either (A) LY294002 ( n = 4, ** p < 0.01, *** p < 0.005) or (B) wortmannin ( n = 4, ** p < 0.01, **** p < 0.0001), as well as Akt inhibition using (C) Akt inhibitor VIII ( n = 4, ** p < 0.01). Smad3 signaling downstream of TGFβ1 was assessed by its C-terminal phosphorylation at Ser473/475 (pSmad3). HG (48 h)-induced Smad3 phosphorylation was prevented by (D) LY294002, (E) wortmannin, and (F) Akt inhibitor VIII ( n = 4, * p < 0.05).
    Figure Legend Snippet: HG-induced TGFβ1 activation and signaling are blocked by PI3K/Akt inhibition. HG (48 h)-induced TGFβ1 activation, assessed by ELISA of medium without acid activation, was prevented by PI3K inhibition using either (A) LY294002 ( n = 4, ** p < 0.01, *** p < 0.005) or (B) wortmannin ( n = 4, ** p < 0.01, **** p < 0.0001), as well as Akt inhibition using (C) Akt inhibitor VIII ( n = 4, ** p < 0.01). Smad3 signaling downstream of TGFβ1 was assessed by its C-terminal phosphorylation at Ser473/475 (pSmad3). HG (48 h)-induced Smad3 phosphorylation was prevented by (D) LY294002, (E) wortmannin, and (F) Akt inhibitor VIII ( n = 4, * p < 0.05).

    Techniques Used: Activation Assay, Inhibition, Enzyme-linked Immunosorbent Assay

    Cell surface GRP78 mediates HG-induced TSP1 expression through Akt activation. (A) csGRP78 inhibition using the C38 antibody, but not a control IgG (2 µg for each antibody) prevented HG (24 h)-induced TSP1 transcript upregulation ( n = 6–8, * p < 0.05). HG (48 h)-induced TSP1 promoter activity, assessed using a luciferase reporter construct, was also inhibited by csGRP78 inhibition using either (B) the C38 antibody ( n = 3, ** p < 0.01, *** p < 0.005, **** p < 0.0001) or (C) vaspin ( n = 3, ** p < 0.01, *** p < 0.005, **** p < 0.001). Further, csGRP78 inhibition also prevented HG (48 h)-induced Akt activation assessed by its phosphorylation at Ser473 as well as TSP1 upregulation using (D) C38, but not control IgG, antibody ( n = 5, * p < 0.05, ** p < 0.01), (E) vaspin ( n = 10, * p < 0.05, ** p < 0.01, *** p < 0.005) and (F) siRNA knockdown of MTJ1, the chaperone required for cell surface translocation of GRP78 in HG ( n = 3, * p < 0.05, ** p < 0.01). (G) Antibody neutralization of the known ligand and activator for csGRP78, α2M*, prevented HG (48 h)-induced TSP1 upregulation. Control IgG had no effect (10 µg for each antibody, n = 3, * p < 0.05). (H) An inhibitory peptide (Pep) that prevents the interaction between α2M* and csGRP78 also inhibited TSP1 upregulation by HG (48 h), with scrambled peptide (Scr) having no effect (100 nM, n = 5, * p < 0.05, ** p < 0.01, *** p < 0.005).
    Figure Legend Snippet: Cell surface GRP78 mediates HG-induced TSP1 expression through Akt activation. (A) csGRP78 inhibition using the C38 antibody, but not a control IgG (2 µg for each antibody) prevented HG (24 h)-induced TSP1 transcript upregulation ( n = 6–8, * p < 0.05). HG (48 h)-induced TSP1 promoter activity, assessed using a luciferase reporter construct, was also inhibited by csGRP78 inhibition using either (B) the C38 antibody ( n = 3, ** p < 0.01, *** p < 0.005, **** p < 0.0001) or (C) vaspin ( n = 3, ** p < 0.01, *** p < 0.005, **** p < 0.001). Further, csGRP78 inhibition also prevented HG (48 h)-induced Akt activation assessed by its phosphorylation at Ser473 as well as TSP1 upregulation using (D) C38, but not control IgG, antibody ( n = 5, * p < 0.05, ** p < 0.01), (E) vaspin ( n = 10, * p < 0.05, ** p < 0.01, *** p < 0.005) and (F) siRNA knockdown of MTJ1, the chaperone required for cell surface translocation of GRP78 in HG ( n = 3, * p < 0.05, ** p < 0.01). (G) Antibody neutralization of the known ligand and activator for csGRP78, α2M*, prevented HG (48 h)-induced TSP1 upregulation. Control IgG had no effect (10 µg for each antibody, n = 3, * p < 0.05). (H) An inhibitory peptide (Pep) that prevents the interaction between α2M* and csGRP78 also inhibited TSP1 upregulation by HG (48 h), with scrambled peptide (Scr) having no effect (100 nM, n = 5, * p < 0.05, ** p < 0.01, *** p < 0.005).

    Techniques Used: Expressing, Activation Assay, Inhibition, Activity Assay, Luciferase, Construct, Translocation Assay, Neutralization

    Proposed role for csGRP78 in mediated TGFβ1 activation through regulation of TSP1 in MC. HG promotes GRP78 localization on the cell surface. Increased activation of the protease inhibitor α2M (denoted α2M*) enables its high-affinity interaction with csGRP78. This induces downstream PI3K/Akt activation and consequent TSP1 gene upregulation. The increased TSP1 localizes to the ECM, where others have shown it to interact with latent TGFβ1 and serve as an important regulator of TGFβ1 activation. The nature and role of csGRP78 interaction with this complex requires further study. These data support a role for csGRP78/α2M* in mediating TGFβ1 profibrotic activation in MC by HG, thus highlighting a potential therapeutic target for indirect TGFβ1 inhibition. Created with BioRender.
    Figure Legend Snippet: Proposed role for csGRP78 in mediated TGFβ1 activation through regulation of TSP1 in MC. HG promotes GRP78 localization on the cell surface. Increased activation of the protease inhibitor α2M (denoted α2M*) enables its high-affinity interaction with csGRP78. This induces downstream PI3K/Akt activation and consequent TSP1 gene upregulation. The increased TSP1 localizes to the ECM, where others have shown it to interact with latent TGFβ1 and serve as an important regulator of TGFβ1 activation. The nature and role of csGRP78 interaction with this complex requires further study. These data support a role for csGRP78/α2M* in mediating TGFβ1 profibrotic activation in MC by HG, thus highlighting a potential therapeutic target for indirect TGFβ1 inhibition. Created with BioRender.

    Techniques Used: Activation Assay, Protease Inhibitor, Inhibition

    immunodetection rabbit anti total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc immunodetection rabbit anti total akt
    Immunodetection Rabbit Anti Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt

    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Social isolation exacerbates diet-induced obesity and peripheral inflammation in young male mice under thermoneutrality"

    Article Title: Social isolation exacerbates diet-induced obesity and peripheral inflammation in young male mice under thermoneutrality

    Journal: iScience

    doi: 10.1016/j.isci.2023.106259


    Figure Legend Snippet:

    Techniques Used: Recombinant, Enzyme-linked Immunosorbent Assay, Colorimetric Assay, Software

    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt

    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total akt/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    1) Product Images from "Social isolation exacerbates diet-induced obesity and peripheral inflammation in young male mice under thermoneutrality"

    Article Title: Social isolation exacerbates diet-induced obesity and peripheral inflammation in young male mice under thermoneutrality

    Journal: iScience

    doi: 10.1016/j.isci.2023.106259


    Figure Legend Snippet:

    Techniques Used: Recombinant, Enzyme-linked Immunosorbent Assay, Colorimetric Assay, Software

    total akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc total akt

    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total akt/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    1) Product Images from "Exercise-acclimated microbiota improves skeletal muscle metabolism via circulating bile acid deconjugation"

    Article Title: Exercise-acclimated microbiota improves skeletal muscle metabolism via circulating bile acid deconjugation

    Journal: iScience

    doi: 10.1016/j.isci.2023.106251


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    Techniques Used: Recombinant, Enzyme-linked Immunosorbent Assay, Protein Extraction, Expressing, Software, Mass Spectrometry, Real-time Polymerase Chain Reaction

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    Cell Signaling Technology Inc total akt
    Effects of ADAM12 on oncogenic signaling pathways in the human colorectal cancer cells. Representative western blot images and semi-quantification graphs for the phosphorylation levels of PDK1, GSK-3β and <t>AKT</t> in AV-transfected or AS-transfected DLD1 or SW480 cells. Data are presented as the mean ± SD (n=3). * P<0.05. ADAM12, a disintegrin and metalloprotease 12; PDK1, phosphoinositide-dependent protein kinase 1; <t>GSK-3β,</t> <t>glycogen</t> synthase kinase-3β; EV, empty pcDNA6-myc vector; AV, ADAM12-pcDNA6-myc construct; SS, scrambled siRNA; AS, ADAM12 siRNA; siRNA, small interfering RNA; p-, phosphorylated; T-, total.
    Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total akt/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc anti total akt
    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling <t>pathways</t> <t>ERK1/2,</t> <t>Akt</t> and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .
    Anti Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti total akt/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti total akt - by Bioz Stars, 2023-03
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    Cell Signaling Technology Inc immunodetection rabbit anti total akt
    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling <t>pathways</t> <t>ERK1/2,</t> <t>Akt</t> and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .
    Immunodetection Rabbit Anti Total Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/immunodetection rabbit anti total akt/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    immunodetection rabbit anti total akt - by Bioz Stars, 2023-03
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    Image Search Results


    Effects of ADAM12 on oncogenic signaling pathways in the human colorectal cancer cells. Representative western blot images and semi-quantification graphs for the phosphorylation levels of PDK1, GSK-3β and AKT in AV-transfected or AS-transfected DLD1 or SW480 cells. Data are presented as the mean ± SD (n=3). * P<0.05. ADAM12, a disintegrin and metalloprotease 12; PDK1, phosphoinositide-dependent protein kinase 1; GSK-3β, glycogen synthase kinase-3β; EV, empty pcDNA6-myc vector; AV, ADAM12-pcDNA6-myc construct; SS, scrambled siRNA; AS, ADAM12 siRNA; siRNA, small interfering RNA; p-, phosphorylated; T-, total.

    Journal: International Journal of Oncology

    Article Title: A disintegrin and metalloprotease 12 contributes to colorectal cancer metastasis by regulating epithelial-mesenchymal transition

    doi: 10.3892/ijo.2023.5498

    Figure Lengend Snippet: Effects of ADAM12 on oncogenic signaling pathways in the human colorectal cancer cells. Representative western blot images and semi-quantification graphs for the phosphorylation levels of PDK1, GSK-3β and AKT in AV-transfected or AS-transfected DLD1 or SW480 cells. Data are presented as the mean ± SD (n=3). * P<0.05. ADAM12, a disintegrin and metalloprotease 12; PDK1, phosphoinositide-dependent protein kinase 1; GSK-3β, glycogen synthase kinase-3β; EV, empty pcDNA6-myc vector; AV, ADAM12-pcDNA6-myc construct; SS, scrambled siRNA; AS, ADAM12 siRNA; siRNA, small interfering RNA; p-, phosphorylated; T-, total.

    Article Snippet: Antibodies against E-cadherin (cat. no. #14472), Snail (cat. no. #3879), vimentin (cat. no. #5741), claudin-1 (cat. no. #4933), integrin α5 (cat. no. #4705), integrin β1 (cat. no. #9699), integrin β3 (cat. no. #13166), phosphorylated (p)-AKT (S473) (cat. no. #4060), p-phosphoinositide-dependent protein kinase 1 (PDK1) (S241) (cat. no. #3438), p-glycogen synthase kinase-3β (GSK-3β) (S9) (cat. no. #9323), total AKT (cat. no. #4691), total PDK1 (cat. no. #3062), total GSK-3β (cat. no. #9832) and Myc-tag (cat. no. #2278) were obtained from Cell Signaling Technology, Inc. Antibodies against β-tubulin (cat. no. sc-9104) and GAPDH (cat. no. sc-25778) were purchased from Santa Cruz Biotechnology, Inc.

    Techniques: Western Blot, Transfection, Plasmid Preparation, Construct, Small Interfering RNA

    Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, Akt and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .

    Journal: Cancers

    Article Title: 2-Arachidonoylglycerol Modulates CXCL12-Mediated Chemotaxis in Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia

    doi: 10.3390/cancers15051585

    Figure Lengend Snippet: Activation of signaling pathways. ( A ) JeKo-1, ( B ) Granta519 and ( C ) JVM-2 were incubated for 2 min with CXCL12 (200 ng/mL) or 2-AG (100 nM) or the combination, and the activation of the signaling pathways ERK1/2, Akt and p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of at least four repeats and error bars are standard error of the mean; paired t -test, * p < 0.05, ** p < 0.01, *** p < 0.001, ns: non-significant, a representative blot for each experiment is shown. Original blot see .

    Article Snippet: Antibodies used for Western blotting: anti-phospho ERK1/2 (Thr202/Tyr204), anti-total ERK1/2, anti-phospho p38 (Thr180/Tyr182), anti-total p38, anti-phospho Akt (Ser473) and anti-total Akt were all from Cell Signaling Technology (Danvers, MA, USA).

    Techniques: Activation Assay, Incubation, Western Blot

    Effects of inhibiting the cannabinoid receptors on Akt and p38 activation. JeKo-1 cells were treated for 20 min with the CB1 antagonist SR141716 (10 nM), or with the CB2 inverse agonist SR1445282 (10 nM), prior to be incubated for 2 min with 2-AG. Activation of the signaling pathways ( A ) Akt and ( B ) p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of three repeats and error bars are standard error of the mean; 2-AG condition is shown as normalized to incubation with vehicle set as 1, unpaired t -test with Welch’s correction, # p < 0.05.

    Journal: Cancers

    Article Title: 2-Arachidonoylglycerol Modulates CXCL12-Mediated Chemotaxis in Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia

    doi: 10.3390/cancers15051585

    Figure Lengend Snippet: Effects of inhibiting the cannabinoid receptors on Akt and p38 activation. JeKo-1 cells were treated for 20 min with the CB1 antagonist SR141716 (10 nM), or with the CB2 inverse agonist SR1445282 (10 nM), prior to be incubated for 2 min with 2-AG. Activation of the signaling pathways ( A ) Akt and ( B ) p38 was assessed by Western blotting, normalizing phospho/GAPDH band intensity to total/GAPDH as described in , bars represent an average of the ratio of three repeats and error bars are standard error of the mean; 2-AG condition is shown as normalized to incubation with vehicle set as 1, unpaired t -test with Welch’s correction, # p < 0.05.

    Article Snippet: Antibodies used for Western blotting: anti-phospho ERK1/2 (Thr202/Tyr204), anti-total ERK1/2, anti-phospho p38 (Thr180/Tyr182), anti-total p38, anti-phospho Akt (Ser473) and anti-total Akt were all from Cell Signaling Technology (Danvers, MA, USA).

    Techniques: Activation Assay, Incubation, Western Blot