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primary antibodies against atrap  (Bethyl)


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    Structured Review

    Bethyl primary antibodies against atrap
    Expression and localization of angiotensin II type 1 receptor-associated protein <t>(ATRAP)</t> in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.
    Primary Antibodies Against Atrap, supplied by Bethyl, used in various techniques. Bioz Stars score: 95/100, based on 215 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against atrap/product/Bethyl
    Average 95 stars, based on 215 article reviews
    primary antibodies against atrap - by Bioz Stars, 2026-02
    95/100 stars

    Images

    1) Product Images from "Effects of proximal tubule-specific ATRAP enhancement on hypertension in a remnant kidney chronic kidney disease model of mice"

    Article Title: Effects of proximal tubule-specific ATRAP enhancement on hypertension in a remnant kidney chronic kidney disease model of mice

    Journal: Scientific Reports

    doi: 10.1038/s41598-025-12168-3

    Expression and localization of angiotensin II type 1 receptor-associated protein (ATRAP) in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.
    Figure Legend Snippet: Expression and localization of angiotensin II type 1 receptor-associated protein (ATRAP) in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.

    Techniques Used: Expressing, Transgenic Assay, Control, Western Blot, Staining, Marker, Laser Capture Microdissection



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    Bethyl primary antibodies against atrap
    Expression and localization of angiotensin II type 1 receptor-associated protein <t>(ATRAP)</t> in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.
    Primary Antibodies Against Atrap, supplied by Bethyl, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against atrap/product/Bethyl
    Average 95 stars, based on 1 article reviews
    primary antibodies against atrap - by Bioz Stars, 2026-02
    95/100 stars
      Buy from Supplier

    90
    Cell Signaling Technology Inc primary antibodies against atrap
    Expression and localization of angiotensin II type 1 receptor-associated protein <t>(ATRAP)</t> in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.
    Primary Antibodies Against Atrap, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against atrap/product/Cell Signaling Technology Inc
    Average 90 stars, based on 1 article reviews
    primary antibodies against atrap - by Bioz Stars, 2026-02
    90/100 stars
      Buy from Supplier

    Image Search Results


    Expression and localization of angiotensin II type 1 receptor-associated protein (ATRAP) in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.

    Journal: Scientific Reports

    Article Title: Effects of proximal tubule-specific ATRAP enhancement on hypertension in a remnant kidney chronic kidney disease model of mice

    doi: 10.1038/s41598-025-12168-3

    Figure Lengend Snippet: Expression and localization of angiotensin II type 1 receptor-associated protein (ATRAP) in proximal tubule-specific ATRAP transgenic (PT-Tg) and littermate-control (LC) mice. (a) Representative western blots and quantitative analysis of ATRAP in the kidney of littermate-control (LC) and proximal tubule-specific ATRAP transgenic (PT-Tg) mice. Values are expressed as mean ± SEM (n = 5 in each group). *** P < 0.001 versus LC, unpaired t -test. (b) Renal cortical sections showing ATRAP expression in renal tubules detected by anti-ATRAP antibody (left panels). Consecutive sections were stained with a monoclonal antibody against megalin (middle panels), a specific marker of proximal tubule (PT), and a monoclonal antibody against calbindin-D (right panels), a specific marker of distal convoluted tubule (DT) and connecting tubule. Original magnification: × 400. (c, d, e) Quantitative analysis of calbindin-D, megalin and ATRAP mRNA expression in Glo, PTs, and DTs of the renal cortex identified by the LMD method. Values are normalized relative to 18S rRNA control levels. Values are expressed as mean ± SEM (n = 4 mice in mix). ATRAP, Angiotensin II type 1 receptor-associated protein; LC, littermate-control; PT-Tg, proximal tubule-specific ATRAP transgenic; Glo, glomerulus; PT, proximal tubule; DT, distal tubule; LMD, Laser‐capture microdissection.

    Article Snippet: Samples were run on a 5–20% polyacrylamide gel, transferred to PVDF membranes, blocked, and probed with specific primary antibodies against ATRAP (diluted 1:2000, developed in our laboratory as previously described – ), HA (diluted 3:2000, A190-108A-2; Bethyl Laboratories, Montgomery, TX, USA) and GAPDH (diluted 1:2000, GTX100118; GeneTex, Irvine, CA, USA).

    Techniques: Expressing, Transgenic Assay, Control, Western Blot, Staining, Marker, Laser Capture Microdissection