arginine vasopressin avp receptor 2  (Alomone Labs)


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    Alomone Labs arginine vasopressin avp receptor 2
    CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma <t>AVP</t> levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).
    Arginine Vasopressin Avp Receptor 2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/arginine vasopressin avp receptor 2/product/Alomone Labs
    Average 94 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    arginine vasopressin avp receptor 2 - by Bioz Stars, 2022-10
    94/100 stars

    Images

    1) Product Images from "Medullary thick ascending limb impairment in the GlatmTg(CAG-A4GALT) Fabry model mice"

    Article Title: Medullary thick ascending limb impairment in the GlatmTg(CAG-A4GALT) Fabry model mice

    Journal: The FASEB Journal

    doi: 10.1096/fj.201701374R

    CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma AVP levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).
    Figure Legend Snippet: CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma AVP levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).

    Techniques Used: Transmission Assay, Mouse Assay, Quantitative RT-PCR, Western Blot, Immunocytochemistry, Expressing, Whisker Assay

    2) Product Images from "Medullary thick ascending limb impairment in the GlatmTg(CAG-A4GALT) Fabry model mice"

    Article Title: Medullary thick ascending limb impairment in the GlatmTg(CAG-A4GALT) Fabry model mice

    Journal: The FASEB Journal

    doi: 10.1096/fj.201701374R

    CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma AVP levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).
    Figure Legend Snippet: CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma AVP levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).

    Techniques Used: Transmission Assay, Mouse Assay, Quantitative RT-PCR, Western Blot, Immunocytochemistry, Expressing, Whisker Assay

    3) Product Images from "Anti-stress Effect of Octopus Cephalotocin in Rats"

    Article Title: Anti-stress Effect of Octopus Cephalotocin in Rats

    Journal: Experimental Neurobiology

    doi: 10.5607/en22010

    Avpr1b was generally expressed at high levels in the hippocampus. (a) Bright field images of the amygdala, (b) hippocampal CA1 region, (c) hippocampal CA3 region, (d) retrosplenial cortex, (e) hypothalamus. (f) Avpr1b expression in the amygdala. (g) Avpr1b expression in the hippocampal CA1 region. (h) Avpr1b expression in the hippocampal CA3 region. (i) Avpr1b expression in the retrosplenial cortex. (j) Avpr1b expression in the hypothalamus. (k) DAPI and Avpr1b staining in the amygdala. (l) DAPI and Avpr1b staining in the hippocampal CA1 region. (m) DAPI and Avpr1b staining in the hippocampal CA3 region. (n) DAPI and Avpr1b staining in the retrosplenial cortex. (o) DAPI and Avpr1b staining in the hypothalamus. (p) Bar graph summarizing the number of Avpr1b puncta. (q) Bar graph summarizing the number of DAPI-stained. (r) Ratio (number of red puncta/number of blue-stained regions) showing that Avpr1b was expressed at high levels in the hippocampus.
    Figure Legend Snippet: Avpr1b was generally expressed at high levels in the hippocampus. (a) Bright field images of the amygdala, (b) hippocampal CA1 region, (c) hippocampal CA3 region, (d) retrosplenial cortex, (e) hypothalamus. (f) Avpr1b expression in the amygdala. (g) Avpr1b expression in the hippocampal CA1 region. (h) Avpr1b expression in the hippocampal CA3 region. (i) Avpr1b expression in the retrosplenial cortex. (j) Avpr1b expression in the hypothalamus. (k) DAPI and Avpr1b staining in the amygdala. (l) DAPI and Avpr1b staining in the hippocampal CA1 region. (m) DAPI and Avpr1b staining in the hippocampal CA3 region. (n) DAPI and Avpr1b staining in the retrosplenial cortex. (o) DAPI and Avpr1b staining in the hypothalamus. (p) Bar graph summarizing the number of Avpr1b puncta. (q) Bar graph summarizing the number of DAPI-stained. (r) Ratio (number of red puncta/number of blue-stained regions) showing that Avpr1b was expressed at high levels in the hippocampus.

    Techniques Used: Expressing, Staining

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    Alomone Labs arginine vasopressin avp receptor 2
    CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma <t>AVP</t> levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).
    Arginine Vasopressin Avp Receptor 2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/arginine vasopressin avp receptor 2/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    arginine vasopressin avp receptor 2 - by Bioz Stars, 2022-10
    94/100 stars
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    CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma AVP levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).

    Journal: The FASEB Journal

    Article Title: Medullary thick ascending limb impairment in the GlatmTg(CAG-A4GALT) Fabry model mice

    doi: 10.1096/fj.201701374R

    Figure Lengend Snippet: CD response to TAL dysfunction. A ) Representative transmission electron micrographs of a CD in the inner medulla in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrowheads indicate a lamellar body. Scale bars, 1 μm. B ) Real-time RT-PCR analysis of Aqp2 levels in the same mice as in Fig. 4 A . C ) Representative (of 2 experiments) Western blot analysis of AQP2 in the same mice as in Fig. 4 B . D ) Representative images of a PC-specific transporter (AQP2) in a CD of Gla tm Tg(CAG-A4GALT) and WT mice ( n = 3/group). Arrows indicate a swollen PC. Arrowheads indicate an ICC. Scale bars, 10 μm. E ) Plasma AVP levels in 20-wk-old Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). F ) Representative (of 2 experiments) Western blot analysis of AVP receptor 2 (AVPR2) expression in Gla tm Tg(CAG-A4GALT) and WT mice ( n = 6/group). In box-and-whisker plots ( B , C , E , F ), center lines represent the median, limits represent quartiles, whiskers represent the 10th and 90th percentiles, and red lines represent the mean. Differences between groups were evaluated by using Student’s t test; data are shown as t (integral degree of freedom) = t , P . For Welch’s t test, data are shown as t (mixed decimal degree of freedom) = t , P . For the Wilcoxon rank-sum test, data are shown with a P value only. ICC, intercalated cell (mitochondria-rich, dark cell); PC, principal cell (light cell).

    Article Snippet: Abs against the following proteins were used: UMOD (AbD Serotec), NKCC2 (Alpha Diagnostic International, San Antonio, TX, USA), Na+ -K+-ATPase (Abcam), NCC (EMD Millipore), AQP2 (Abcam), arginine vasopressin (AVP) receptor 2 (Alomone Labs, Jerusalem, Israel), and GAPDH (MilliporeSigma, St. Louis, MO, USA).

    Techniques: Transmission Assay, Mouse Assay, Quantitative RT-PCR, Western Blot, Immunocytochemistry, Expressing, Whisker Assay

    Avpr1b was generally expressed at high levels in the hippocampus. (a) Bright field images of the amygdala, (b) hippocampal CA1 region, (c) hippocampal CA3 region, (d) retrosplenial cortex, (e) hypothalamus. (f) Avpr1b expression in the amygdala. (g) Avpr1b expression in the hippocampal CA1 region. (h) Avpr1b expression in the hippocampal CA3 region. (i) Avpr1b expression in the retrosplenial cortex. (j) Avpr1b expression in the hypothalamus. (k) DAPI and Avpr1b staining in the amygdala. (l) DAPI and Avpr1b staining in the hippocampal CA1 region. (m) DAPI and Avpr1b staining in the hippocampal CA3 region. (n) DAPI and Avpr1b staining in the retrosplenial cortex. (o) DAPI and Avpr1b staining in the hypothalamus. (p) Bar graph summarizing the number of Avpr1b puncta. (q) Bar graph summarizing the number of DAPI-stained. (r) Ratio (number of red puncta/number of blue-stained regions) showing that Avpr1b was expressed at high levels in the hippocampus.

    Journal: Experimental Neurobiology

    Article Title: Anti-stress Effect of Octopus Cephalotocin in Rats

    doi: 10.5607/en22010

    Figure Lengend Snippet: Avpr1b was generally expressed at high levels in the hippocampus. (a) Bright field images of the amygdala, (b) hippocampal CA1 region, (c) hippocampal CA3 region, (d) retrosplenial cortex, (e) hypothalamus. (f) Avpr1b expression in the amygdala. (g) Avpr1b expression in the hippocampal CA1 region. (h) Avpr1b expression in the hippocampal CA3 region. (i) Avpr1b expression in the retrosplenial cortex. (j) Avpr1b expression in the hypothalamus. (k) DAPI and Avpr1b staining in the amygdala. (l) DAPI and Avpr1b staining in the hippocampal CA1 region. (m) DAPI and Avpr1b staining in the hippocampal CA3 region. (n) DAPI and Avpr1b staining in the retrosplenial cortex. (o) DAPI and Avpr1b staining in the hypothalamus. (p) Bar graph summarizing the number of Avpr1b puncta. (q) Bar graph summarizing the number of DAPI-stained. (r) Ratio (number of red puncta/number of blue-stained regions) showing that Avpr1b was expressed at high levels in the hippocampus.

    Article Snippet: The primary antibody, anti-Avpr1b (AVR-011, Alomone, Jerusalem, Israel), was diluted 1:200, and the secondary antibody, Alexa Fluor 594-conjugated goat anti-rabbit (A11012, Invitrogen, MA, USA), was diluted 1:1,000.

    Techniques: Expressing, Staining