anti tsh receptor tshr extracellular antibody  (Alomone Labs)


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    Alomone Labs anti tsh receptor tshr extracellular antibody
    Activation of <t>TSH-R</t> on podocytes is detrimental. (a) qPCR data showing the average Ct value from 2 independent wells for <t>tshr</t> gene in mouse podocytes and mouse thyroid in comparison to the housekeeping gene gapdh . (b) Western blot analysis of lysates from mouse podocytes, mouse thyroid tissue (positive control) and human K562 cells (negative control) probed with the indicated antibodies. Representative blot from two independent experiments is shown. Migration of molecular weight standards is depicted on the left as kDa. (c) Histogram depicting the data from flow cytometric analysis performed on mouse podocytes with FITC-conjugated TSH-R antibody (blue) overlapped with the controls (unstained, red and FITC-conjugated IgG2a isotype control, green). 5000 events were collected and gated. Graph on the right shows the geometric mean fluorescence intensity (MFI) on Y-axis obtained from four independent experiments. Non-parametric two-tailed Students t -test was used to calculate the significance, * p≤0.05 . (d) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), Normal rabbit IgG isotype or anti-TSH-R antibody (3 µg/ml each) for 24 h. Stains: merge of F-actin phalloidin-488 stained in green and DAPI in blue. Scale bar=20 µm. (e) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), or TSH (25 and 50 nM) for 24 h. Stains: merge of F-actin phalloidin-488 in green and DAPI in blue. Scale bar=20 µm. (f) Quantification of the data in d, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, ** p≤0.01 and *** p≤0.001 . (g) Quantification of the data in e, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 . (h) cAMP levels (in pmol/ml) normalized with the protein concentration (mg/ml), plotted as pmol/mg in the culture supernatants of mouse podocytes exposed to the indicated treatments for 60 min. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 and * p≤0.05 . (i) qPCR analysis of DIO3 transcript in mouse podocytes upon PAN (30 µg/ml) and TSH (25 and 50 nM) treatment for 24 h. gapdh was used as the housekeeping gene; ** p≤0.01 and * p≤0.05 determined using non-parametric Students t -test.
    Anti Tsh Receptor Tshr Extracellular 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 tsh receptor tshr extracellular antibody/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti tsh receptor tshr extracellular antibody - by Bioz Stars, 2022-12
    93/100 stars

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    1) Product Images from "Deiodinase-3 is a thyrostat to regulate podocyte homeostasis"

    Article Title: Deiodinase-3 is a thyrostat to regulate podocyte homeostasis

    Journal: EBioMedicine

    doi: 10.1016/j.ebiom.2021.103617

    Activation of TSH-R on podocytes is detrimental. (a) qPCR data showing the average Ct value from 2 independent wells for tshr gene in mouse podocytes and mouse thyroid in comparison to the housekeeping gene gapdh . (b) Western blot analysis of lysates from mouse podocytes, mouse thyroid tissue (positive control) and human K562 cells (negative control) probed with the indicated antibodies. Representative blot from two independent experiments is shown. Migration of molecular weight standards is depicted on the left as kDa. (c) Histogram depicting the data from flow cytometric analysis performed on mouse podocytes with FITC-conjugated TSH-R antibody (blue) overlapped with the controls (unstained, red and FITC-conjugated IgG2a isotype control, green). 5000 events were collected and gated. Graph on the right shows the geometric mean fluorescence intensity (MFI) on Y-axis obtained from four independent experiments. Non-parametric two-tailed Students t -test was used to calculate the significance, * p≤0.05 . (d) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), Normal rabbit IgG isotype or anti-TSH-R antibody (3 µg/ml each) for 24 h. Stains: merge of F-actin phalloidin-488 stained in green and DAPI in blue. Scale bar=20 µm. (e) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), or TSH (25 and 50 nM) for 24 h. Stains: merge of F-actin phalloidin-488 in green and DAPI in blue. Scale bar=20 µm. (f) Quantification of the data in d, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, ** p≤0.01 and *** p≤0.001 . (g) Quantification of the data in e, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 . (h) cAMP levels (in pmol/ml) normalized with the protein concentration (mg/ml), plotted as pmol/mg in the culture supernatants of mouse podocytes exposed to the indicated treatments for 60 min. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 and * p≤0.05 . (i) qPCR analysis of DIO3 transcript in mouse podocytes upon PAN (30 µg/ml) and TSH (25 and 50 nM) treatment for 24 h. gapdh was used as the housekeeping gene; ** p≤0.01 and * p≤0.05 determined using non-parametric Students t -test.
    Figure Legend Snippet: Activation of TSH-R on podocytes is detrimental. (a) qPCR data showing the average Ct value from 2 independent wells for tshr gene in mouse podocytes and mouse thyroid in comparison to the housekeeping gene gapdh . (b) Western blot analysis of lysates from mouse podocytes, mouse thyroid tissue (positive control) and human K562 cells (negative control) probed with the indicated antibodies. Representative blot from two independent experiments is shown. Migration of molecular weight standards is depicted on the left as kDa. (c) Histogram depicting the data from flow cytometric analysis performed on mouse podocytes with FITC-conjugated TSH-R antibody (blue) overlapped with the controls (unstained, red and FITC-conjugated IgG2a isotype control, green). 5000 events were collected and gated. Graph on the right shows the geometric mean fluorescence intensity (MFI) on Y-axis obtained from four independent experiments. Non-parametric two-tailed Students t -test was used to calculate the significance, * p≤0.05 . (d) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), Normal rabbit IgG isotype or anti-TSH-R antibody (3 µg/ml each) for 24 h. Stains: merge of F-actin phalloidin-488 stained in green and DAPI in blue. Scale bar=20 µm. (e) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), or TSH (25 and 50 nM) for 24 h. Stains: merge of F-actin phalloidin-488 in green and DAPI in blue. Scale bar=20 µm. (f) Quantification of the data in d, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, ** p≤0.01 and *** p≤0.001 . (g) Quantification of the data in e, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 . (h) cAMP levels (in pmol/ml) normalized with the protein concentration (mg/ml), plotted as pmol/mg in the culture supernatants of mouse podocytes exposed to the indicated treatments for 60 min. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 and * p≤0.05 . (i) qPCR analysis of DIO3 transcript in mouse podocytes upon PAN (30 µg/ml) and TSH (25 and 50 nM) treatment for 24 h. gapdh was used as the housekeeping gene; ** p≤0.01 and * p≤0.05 determined using non-parametric Students t -test.

    Techniques Used: Activation Assay, Real-time Polymerase Chain Reaction, Western Blot, Positive Control, Negative Control, Migration, Molecular Weight, Fluorescence, Two Tailed Test, Cell Culture, Staining, Protein Concentration

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    • anti tsh receptor tshr extracellular antibody  (Alomone Labs)
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    Alomone Labs anti tsh receptor tshr extracellular antibody
    Activation of <t>TSH-R</t> on podocytes is detrimental. (a) qPCR data showing the average Ct value from 2 independent wells for <t>tshr</t> gene in mouse podocytes and mouse thyroid in comparison to the housekeeping gene gapdh . (b) Western blot analysis of lysates from mouse podocytes, mouse thyroid tissue (positive control) and human K562 cells (negative control) probed with the indicated antibodies. Representative blot from two independent experiments is shown. Migration of molecular weight standards is depicted on the left as kDa. (c) Histogram depicting the data from flow cytometric analysis performed on mouse podocytes with FITC-conjugated TSH-R antibody (blue) overlapped with the controls (unstained, red and FITC-conjugated IgG2a isotype control, green). 5000 events were collected and gated. Graph on the right shows the geometric mean fluorescence intensity (MFI) on Y-axis obtained from four independent experiments. Non-parametric two-tailed Students t -test was used to calculate the significance, * p≤0.05 . (d) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), Normal rabbit IgG isotype or anti-TSH-R antibody (3 µg/ml each) for 24 h. Stains: merge of F-actin phalloidin-488 stained in green and DAPI in blue. Scale bar=20 µm. (e) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), or TSH (25 and 50 nM) for 24 h. Stains: merge of F-actin phalloidin-488 in green and DAPI in blue. Scale bar=20 µm. (f) Quantification of the data in d, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, ** p≤0.01 and *** p≤0.001 . (g) Quantification of the data in e, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 . (h) cAMP levels (in pmol/ml) normalized with the protein concentration (mg/ml), plotted as pmol/mg in the culture supernatants of mouse podocytes exposed to the indicated treatments for 60 min. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 and * p≤0.05 . (i) qPCR analysis of DIO3 transcript in mouse podocytes upon PAN (30 µg/ml) and TSH (25 and 50 nM) treatment for 24 h. gapdh was used as the housekeeping gene; ** p≤0.01 and * p≤0.05 determined using non-parametric Students t -test.
    Anti Tsh Receptor Tshr Extracellular 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 tsh receptor tshr extracellular antibody/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti tsh receptor tshr extracellular antibody - by Bioz Stars, 2022-12
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    Activation of TSH-R on podocytes is detrimental. (a) qPCR data showing the average Ct value from 2 independent wells for tshr gene in mouse podocytes and mouse thyroid in comparison to the housekeeping gene gapdh . (b) Western blot analysis of lysates from mouse podocytes, mouse thyroid tissue (positive control) and human K562 cells (negative control) probed with the indicated antibodies. Representative blot from two independent experiments is shown. Migration of molecular weight standards is depicted on the left as kDa. (c) Histogram depicting the data from flow cytometric analysis performed on mouse podocytes with FITC-conjugated TSH-R antibody (blue) overlapped with the controls (unstained, red and FITC-conjugated IgG2a isotype control, green). 5000 events were collected and gated. Graph on the right shows the geometric mean fluorescence intensity (MFI) on Y-axis obtained from four independent experiments. Non-parametric two-tailed Students t -test was used to calculate the significance, * p≤0.05 . (d) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), Normal rabbit IgG isotype or anti-TSH-R antibody (3 µg/ml each) for 24 h. Stains: merge of F-actin phalloidin-488 stained in green and DAPI in blue. Scale bar=20 µm. (e) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), or TSH (25 and 50 nM) for 24 h. Stains: merge of F-actin phalloidin-488 in green and DAPI in blue. Scale bar=20 µm. (f) Quantification of the data in d, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, ** p≤0.01 and *** p≤0.001 . (g) Quantification of the data in e, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 . (h) cAMP levels (in pmol/ml) normalized with the protein concentration (mg/ml), plotted as pmol/mg in the culture supernatants of mouse podocytes exposed to the indicated treatments for 60 min. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 and * p≤0.05 . (i) qPCR analysis of DIO3 transcript in mouse podocytes upon PAN (30 µg/ml) and TSH (25 and 50 nM) treatment for 24 h. gapdh was used as the housekeeping gene; ** p≤0.01 and * p≤0.05 determined using non-parametric Students t -test.

    Journal: EBioMedicine

    Article Title: Deiodinase-3 is a thyrostat to regulate podocyte homeostasis

    doi: 10.1016/j.ebiom.2021.103617

    Figure Lengend Snippet: Activation of TSH-R on podocytes is detrimental. (a) qPCR data showing the average Ct value from 2 independent wells for tshr gene in mouse podocytes and mouse thyroid in comparison to the housekeeping gene gapdh . (b) Western blot analysis of lysates from mouse podocytes, mouse thyroid tissue (positive control) and human K562 cells (negative control) probed with the indicated antibodies. Representative blot from two independent experiments is shown. Migration of molecular weight standards is depicted on the left as kDa. (c) Histogram depicting the data from flow cytometric analysis performed on mouse podocytes with FITC-conjugated TSH-R antibody (blue) overlapped with the controls (unstained, red and FITC-conjugated IgG2a isotype control, green). 5000 events were collected and gated. Graph on the right shows the geometric mean fluorescence intensity (MFI) on Y-axis obtained from four independent experiments. Non-parametric two-tailed Students t -test was used to calculate the significance, * p≤0.05 . (d) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), Normal rabbit IgG isotype or anti-TSH-R antibody (3 µg/ml each) for 24 h. Stains: merge of F-actin phalloidin-488 stained in green and DAPI in blue. Scale bar=20 µm. (e) Confocal micrographs of cultured mouse podocytes left untreated (UT), PAN treated (30 µg/ml), or TSH (25 and 50 nM) for 24 h. Stains: merge of F-actin phalloidin-488 in green and DAPI in blue. Scale bar=20 µm. (f) Quantification of the data in d, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, ** p≤0.01 and *** p≤0.001 . (g) Quantification of the data in e, represented as percentage of cells with normal cell shape and size with transversal stress fibers. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 . (h) cAMP levels (in pmol/ml) normalized with the protein concentration (mg/ml), plotted as pmol/mg in the culture supernatants of mouse podocytes exposed to the indicated treatments for 60 min. Non-parametric two-tailed Students t -test was used to calculate the significance, *** p≤0.001 and * p≤0.05 . (i) qPCR analysis of DIO3 transcript in mouse podocytes upon PAN (30 µg/ml) and TSH (25 and 50 nM) treatment for 24 h. gapdh was used as the housekeeping gene; ** p≤0.01 and * p≤0.05 determined using non-parametric Students t -test.

    Article Snippet: Anti-TSH Receptor (TSH-R) (extracellular) Antibody (# ATR-006; RRID:AB_2341080) was from Alomone Labs.

    Techniques: Activation Assay, Real-time Polymerase Chain Reaction, Western Blot, Positive Control, Negative Control, Migration, Molecular Weight, Fluorescence, Two Tailed Test, Cell Culture, Staining, Protein Concentration