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rabbit anti tsh r fitc conjugated antibody  (Bioss)


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    Bioss rabbit anti tsh r fitc conjugated antibody
    Activation of <t>TSH-R</t> 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 <t>FITC-conjugated</t> 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.
    Rabbit Anti Tsh R Fitc Conjugated Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+tshr+polyclonal+antibody/TSHR+Polyclonal+Antibody%2C+FITC+Conjugated/pmc08517284-70-21-25
    Average 91 stars, based on 1 article reviews
    rabbit anti tsh r fitc conjugated antibody - by Bioz Stars, 2026-09
    91/100 stars

    Images

    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, Western Blot, Positive Control, Negative Control, Migration, Molecular Weight, Fluorescence, Two Tailed Test, Cell Culture, Staining, Protein Concentration

    Related Articles

    other:

    Article Title: Genetic immunization with mouse thyrotrophin hormone receptor plasmid breaks self‐tolerance for a murine model of autoimmune thyroid disease and Graves' orbitopathy
    Article Snippet: Assessment of thyroid disease and GO Total thyroxine (T4) was measured using 50 μl serum by enzyme‐linked immunosorbent assay (ELISA) (DRG Diagnostics GmbH, Marburg, Germany).

    Article Title: Genetic immunization with mouse thyrotrophin hormone receptor plasmid breaks self‐tolerance for a murine model of autoimmune thyroid disease and Graves' orbitopathy
    Article Snippet: Total thyroxine (T4) was measured using 50 μl serum by enzyme‐linked immunosorbent assay (ELISA) (DRG Diagnostics GmbH, Marburg, Germany).

    Incubation:

    Article Title: MALAT1 rs619586 polymorphism functions as a prognostic biomarker in the management of differentiated thyroid carcinoma.
    Article Snippet: Correspondence Jun‐xiao Liu, Department of Clinical Laboratory, Luoyang Central Hospital Affiliated to Zhengzhou University, No. 288, Zhong zhou Middle Road, Luoyang, 471000 Henan, China.. Email: medheart@yeah.net Abstract This study aimed to explore the roles of miR‐214 and MALAT1 rs619586 polymorphism in the control and survival of differentiated thyroid carcinoma (DTC) via Cox regression analyses.. The levels of MALAT1, miR‐214, and CTNNB1 in different experimental groups were compared to study the interaction among MALAT1, miR‐214, and CTNNB1.

    Concentration Assay:

    Article Title: MALAT1 rs619586 polymorphism functions as a prognostic biomarker in the management of differentiated thyroid carcinoma.
    Article Snippet: Correspondence Jun‐xiao Liu, Department of Clinical Laboratory, Luoyang Central Hospital Affiliated to Zhengzhou University, No. 288, Zhong zhou Middle Road, Luoyang, 471000 Henan, China.. Email: medheart@yeah.net Abstract This study aimed to explore the roles of miR‐214 and MALAT1 rs619586 polymorphism in the control and survival of differentiated thyroid carcinoma (DTC) via Cox regression analyses.. The levels of MALAT1, miR‐214, and CTNNB1 in different experimental groups were compared to study the interaction among MALAT1, miR‐214, and CTNNB1.

    Bioprocessing:

    Article Title: MALAT1 rs619586 polymorphism functions as a prognostic biomarker in the management of differentiated thyroid carcinoma.
    Article Snippet: Correspondence Jun‐xiao Liu, Department of Clinical Laboratory, Luoyang Central Hospital Affiliated to Zhengzhou University, No. 288, Zhong zhou Middle Road, Luoyang, 471000 Henan, China.. Email: medheart@yeah.net Abstract This study aimed to explore the roles of miR‐214 and MALAT1 rs619586 polymorphism in the control and survival of differentiated thyroid carcinoma (DTC) via Cox regression analyses.. The levels of MALAT1, miR‐214, and CTNNB1 in different experimental groups were compared to study the interaction among MALAT1, miR‐214, and CTNNB1.

    Staining:

    Article Title: MALAT1 rs619586 polymorphism functions as a prognostic biomarker in the management of differentiated thyroid carcinoma.
    Article Snippet: Correspondence Jun‐xiao Liu, Department of Clinical Laboratory, Luoyang Central Hospital Affiliated to Zhengzhou University, No. 288, Zhong zhou Middle Road, Luoyang, 471000 Henan, China.. Email: medheart@yeah.net Abstract This study aimed to explore the roles of miR‐214 and MALAT1 rs619586 polymorphism in the control and survival of differentiated thyroid carcinoma (DTC) via Cox regression analyses.. The levels of MALAT1, miR‐214, and CTNNB1 in different experimental groups were compared to study the interaction among MALAT1, miR‐214, and CTNNB1.



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    Immunofluorescence staining of proteins in thyroid cells using confocal microscopy before differentiation protocol. (A) <t>TSHR</t> (membrane) and (B) TTF1 (nuclear), Thyroid cells stained in green for all proteins and counterstained in blue for nuclei. The cytoskeleton was stained with phalloidin red to observe cell morphology. Objective 40 × original magnification, scale bars represent 50 µm. TSHR = thyroid <t>stimulating</t> hormone receptor, TTF1 = thyroid transcription factor 1.
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    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: In a final volume of 50 µl containing 2 × 10 5 cells, staining was performed with 1:50 dilution of either Rabbit anti-TSH-R-FITC conjugated antibody (Bioss Antibodies, BS-0460R-FITC; RRID:AB_11042712) or normal mouse IgG-FITC (Santa Cruz, sc-2856; RRID:AB_737238) for 1 h at 4°C.

    Techniques: Activation Assay, Western Blot, Positive Control, Negative Control, Migration, Molecular Weight, Fluorescence, Two Tailed Test, Cell Culture, Staining, Protein Concentration

    Immunofluorescence staining of proteins in thyroid cells using confocal microscopy before differentiation protocol. (A) TSHR (membrane) and (B) TTF1 (nuclear), Thyroid cells stained in green for all proteins and counterstained in blue for nuclei. The cytoskeleton was stained with phalloidin red to observe cell morphology. Objective 40 × original magnification, scale bars represent 50 µm. TSHR = thyroid stimulating hormone receptor, TTF1 = thyroid transcription factor 1.

    Journal: Medicine

    Article Title: Production of parathyroid-like cells from thyroid stem cells in co-culture environment

    doi: 10.1097/MD.0000000000032009

    Figure Lengend Snippet: Immunofluorescence staining of proteins in thyroid cells using confocal microscopy before differentiation protocol. (A) TSHR (membrane) and (B) TTF1 (nuclear), Thyroid cells stained in green for all proteins and counterstained in blue for nuclei. The cytoskeleton was stained with phalloidin red to observe cell morphology. Objective 40 × original magnification, scale bars represent 50 µm. TSHR = thyroid stimulating hormone receptor, TTF1 = thyroid transcription factor 1.

    Article Snippet: For immunofluorescence imaging, to visualize cell-specific marker proteins, the following primary and secondary antibodies were used: rabbit polyclonal anti-calcium sensing receptor (CaSR) antibody (Abcam®, ab137408; 1:500), rabbit polyclonal anti-parathyroid hormone receptor 1 (PTH1R) antibody (Abcam®, ab75150; 1:500), rabbit polyclonal anti-thyroid stimulating hormone receptor (TSHR) antibody (Abcam®, ab202960; 1:500), rabbit monoclonal Anti-thyroid transcription factor 1 (TTF1) antibody [SP141] (Abcam®, ab227652; 1:25), mouse monoclonal anti-parathyroid hormone antibody [rPTH/911] (Abcam®, ab234415; 1 μg/mL), goat anti-mouse IgM cross-adsorbed secondary antibody (DyLight® 594) (Invitrogen®, SA5-10152; 1:200) and goat anti-rabbit IgG H&L (Alexa Fluor® 488) (Abcam®, ab150077; 1:1000).

    Techniques: Immunofluorescence, Staining, Confocal Microscopy, Membrane