AQP-002 Search Results


anti aqp2 antibody  (Alomone Labs)
93
Alomone Labs anti aqp2 antibody
Anti Aqp2 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti aqp2 antibody/product/Alomone Labs
Average 93 stars, based on 1 article reviews
anti aqp2 antibody - by Bioz Stars, 2026-04
93/100 stars
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anti aqp2 atto fluor 550  (Alomone Labs)
92
Alomone Labs anti aqp2 atto fluor 550
TRPV4 activity regulates subcellular <t>AQP2</t> distribution in cystic cells of PCK453 rats. (a) Representative confocal images showing AQP2 (pseudocolor red) distribution in kidney sections of PCK453 rats fed regular (0.9%K + ), high KCl (5%K + ), and high KB/C (5%K + , bicarbonate: citrate as 4:1) diets for 1 month. Nuclear Dapi staining is shown with pseudocolor blue. Areas with cystic (1) and non‐dilated collecting duct (2) are shown below at higher magnification. The averaged intensities of AQP2‐reporting fluorescent signals around the apical area in cystic (b) and non‐dilated collecting duct (c) cells from the conditions in (a). For each individual cell the fluorescent signals were normalized to their corresponding maximal value.
Anti Aqp2 Atto Fluor 550, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti aqp2 atto fluor 550/product/Alomone Labs
Average 92 stars, based on 1 article reviews
anti aqp2 atto fluor 550 - by Bioz Stars, 2026-04
92/100 stars
  Buy from Supplier

Image Search Results


TRPV4 activity regulates subcellular AQP2 distribution in cystic cells of PCK453 rats. (a) Representative confocal images showing AQP2 (pseudocolor red) distribution in kidney sections of PCK453 rats fed regular (0.9%K + ), high KCl (5%K + ), and high KB/C (5%K + , bicarbonate: citrate as 4:1) diets for 1 month. Nuclear Dapi staining is shown with pseudocolor blue. Areas with cystic (1) and non‐dilated collecting duct (2) are shown below at higher magnification. The averaged intensities of AQP2‐reporting fluorescent signals around the apical area in cystic (b) and non‐dilated collecting duct (c) cells from the conditions in (a). For each individual cell the fluorescent signals were normalized to their corresponding maximal value.

Journal: Physiological Reports

Article Title: TRPV4 functional status in cystic cells regulates cystogenesis in autosomal recessive polycystic kidney disease during variations in dietary potassium

doi: 10.14814/phy2.15641

Figure Lengend Snippet: TRPV4 activity regulates subcellular AQP2 distribution in cystic cells of PCK453 rats. (a) Representative confocal images showing AQP2 (pseudocolor red) distribution in kidney sections of PCK453 rats fed regular (0.9%K + ), high KCl (5%K + ), and high KB/C (5%K + , bicarbonate: citrate as 4:1) diets for 1 month. Nuclear Dapi staining is shown with pseudocolor blue. Areas with cystic (1) and non‐dilated collecting duct (2) are shown below at higher magnification. The averaged intensities of AQP2‐reporting fluorescent signals around the apical area in cystic (b) and non‐dilated collecting duct (c) cells from the conditions in (a). For each individual cell the fluorescent signals were normalized to their corresponding maximal value.

Article Snippet: Sections were incubated overnight at +4°C with anti‐AQP2‐ATTO Fluor‐550 (1:200, Alomone Labs; Cat. # AQP2‐002‐AO) and anti‐TRPV4 (1:500, Alomone labs; Cat.#.

Techniques: Activity Assay, Staining

TRPV4 activity is inversely related to cAMP levels in cystic cells of PCK453 rats. Summary graph comparing dispersion (decrease by 50% from maximum) of AQP2‐reporting signal in non‐dilated collecting duct versus cystic cells in kidney sections of PCK453 rats fed regular (0.9%K + ), high KCl (5%K + ), and high KB/C (5%K + , bicarbonate: citrate as 4:1) diets for 1 month. Bars and whiskers represent SE and SD, respectively. Mean and median values are denoted with lines. Numbers of each experimental groups are shown below. Kidney sections from at least 4 different animals were used for each tested group. *Significant changes ( p < 0.05, one‐way ANOVA with post hoc Tukey test) between groups shown with brackets on the top.

Journal: Physiological Reports

Article Title: TRPV4 functional status in cystic cells regulates cystogenesis in autosomal recessive polycystic kidney disease during variations in dietary potassium

doi: 10.14814/phy2.15641

Figure Lengend Snippet: TRPV4 activity is inversely related to cAMP levels in cystic cells of PCK453 rats. Summary graph comparing dispersion (decrease by 50% from maximum) of AQP2‐reporting signal in non‐dilated collecting duct versus cystic cells in kidney sections of PCK453 rats fed regular (0.9%K + ), high KCl (5%K + ), and high KB/C (5%K + , bicarbonate: citrate as 4:1) diets for 1 month. Bars and whiskers represent SE and SD, respectively. Mean and median values are denoted with lines. Numbers of each experimental groups are shown below. Kidney sections from at least 4 different animals were used for each tested group. *Significant changes ( p < 0.05, one‐way ANOVA with post hoc Tukey test) between groups shown with brackets on the top.

Article Snippet: Sections were incubated overnight at +4°C with anti‐AQP2‐ATTO Fluor‐550 (1:200, Alomone Labs; Cat. # AQP2‐002‐AO) and anti‐TRPV4 (1:500, Alomone labs; Cat.#.

Techniques: Activity Assay, Dispersion