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fshr mab  (R&D Systems)


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    R&D Systems fshr mab
    Fshr Mab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fshr mab/product/R&D Systems
    Average 92 stars, based on 4 article reviews
    fshr mab - by Bioz Stars, 2026-03
    92/100 stars

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    Effects of CUMS on the relative expression of NGF, TrkA, p75, and FSHR mRNA in the ovarian tissues of CUMS rats. (a) The NGF mRNA expression was affected by CUMS in the ovarian tissue of rats. (b) The TrkA mRNA expression was affected by CUMS in the ovarian tissue of rats. (c) The p75 mRNA expression was affected by CUMS in the ovarian tissue of rats. (d) The FSHR mRNA expression was affected by CUMS in the ovarian tissue of rats. Values are 10 in the control group and 30 in the CUMS group, respectively. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group.

    Journal: BioMed Research International

    Article Title: CUMS Promotes the Development of Premature Ovarian Insufficiency Mediated by Nerve Growth Factor and Its Receptor in Rats

    doi: 10.1155/2020/1946853

    Figure Lengend Snippet: Effects of CUMS on the relative expression of NGF, TrkA, p75, and FSHR mRNA in the ovarian tissues of CUMS rats. (a) The NGF mRNA expression was affected by CUMS in the ovarian tissue of rats. (b) The TrkA mRNA expression was affected by CUMS in the ovarian tissue of rats. (c) The p75 mRNA expression was affected by CUMS in the ovarian tissue of rats. (d) The FSHR mRNA expression was affected by CUMS in the ovarian tissue of rats. Values are 10 in the control group and 30 in the CUMS group, respectively. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group.

    Article Snippet: A blocking solution was added for incubation at 37°C for 1 h. The following primary antibodies were subsequently used: rabbit polyclonal anti-NGF (1 : 100), mouse monoclonal anti-FSHR (1 : 100; Abcam), rabbit polyclonal anti-TrkA (1 : 100), and mouse monoclonal anti-p75 NGF (1 : 100; Abcam).

    Techniques: Expressing

    Effects of CUMS on the expression of NGF, TrkA, p75, and FSHR proteins in the ovarian tissues of rats. (a) The NGF protein expression was affected by CUMS in the ovarian tissue of rats. (b) The TrkA protein expression was affected by CUMS in the ovarian tissue of rats. (c) The p75 protein expression was affected by CUMS in the ovarian tissue of rats. (d) The FSHR protein expression was affected by CUMS in the ovarian tissue of rats. (e) Protein bands for the control and CUMS groups are shown. The molecular weight of TrkA is 150 kDa, FSHR is 77 kDa, p75 is 75 kDa, NGF is 30 kDa, and GAPDH is 38 kDa. Values are 10 in the control group and 30 in the CUMS group, respectively. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group.

    Journal: BioMed Research International

    Article Title: CUMS Promotes the Development of Premature Ovarian Insufficiency Mediated by Nerve Growth Factor and Its Receptor in Rats

    doi: 10.1155/2020/1946853

    Figure Lengend Snippet: Effects of CUMS on the expression of NGF, TrkA, p75, and FSHR proteins in the ovarian tissues of rats. (a) The NGF protein expression was affected by CUMS in the ovarian tissue of rats. (b) The TrkA protein expression was affected by CUMS in the ovarian tissue of rats. (c) The p75 protein expression was affected by CUMS in the ovarian tissue of rats. (d) The FSHR protein expression was affected by CUMS in the ovarian tissue of rats. (e) Protein bands for the control and CUMS groups are shown. The molecular weight of TrkA is 150 kDa, FSHR is 77 kDa, p75 is 75 kDa, NGF is 30 kDa, and GAPDH is 38 kDa. Values are 10 in the control group and 30 in the CUMS group, respectively. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group.

    Article Snippet: A blocking solution was added for incubation at 37°C for 1 h. The following primary antibodies were subsequently used: rabbit polyclonal anti-NGF (1 : 100), mouse monoclonal anti-FSHR (1 : 100; Abcam), rabbit polyclonal anti-TrkA (1 : 100), and mouse monoclonal anti-p75 NGF (1 : 100; Abcam).

    Techniques: Expressing, Molecular Weight

    Immunofluorescence localization of NGF, p75, TrkA, and FSHR proteins in the ovarian tissues of CUMS rats Tissues were stained for NGF using TRITC-labeled secondary antibody (red), and for p75 using FITC-labeled secondary antibody (green). Nuclei were stained using DAPI (blue). Tissues were stained for TrkA using TRITC-labeled secondary antibody (red) and for FSHR using FITC-labeled secondary antibody (green). Nuclei were stained using DAPI (blue). In the figure, the ∗ symbol indicates corpus luteum, ★ indicates antral follicles, ↓and small follicles, and ▲ indicates ovarian stroma, scale bar = 50 μ m. Values are 10 in the control group and 30 in the CUMS group, respectively.

    Journal: BioMed Research International

    Article Title: CUMS Promotes the Development of Premature Ovarian Insufficiency Mediated by Nerve Growth Factor and Its Receptor in Rats

    doi: 10.1155/2020/1946853

    Figure Lengend Snippet: Immunofluorescence localization of NGF, p75, TrkA, and FSHR proteins in the ovarian tissues of CUMS rats Tissues were stained for NGF using TRITC-labeled secondary antibody (red), and for p75 using FITC-labeled secondary antibody (green). Nuclei were stained using DAPI (blue). Tissues were stained for TrkA using TRITC-labeled secondary antibody (red) and for FSHR using FITC-labeled secondary antibody (green). Nuclei were stained using DAPI (blue). In the figure, the ∗ symbol indicates corpus luteum, ★ indicates antral follicles, ↓and small follicles, and ▲ indicates ovarian stroma, scale bar = 50 μ m. Values are 10 in the control group and 30 in the CUMS group, respectively.

    Article Snippet: A blocking solution was added for incubation at 37°C for 1 h. The following primary antibodies were subsequently used: rabbit polyclonal anti-NGF (1 : 100), mouse monoclonal anti-FSHR (1 : 100; Abcam), rabbit polyclonal anti-TrkA (1 : 100), and mouse monoclonal anti-p75 NGF (1 : 100; Abcam).

    Techniques: Immunofluorescence, Staining, Labeling

    The relative expression of TrkA, p75, and FSHR mRNA of CUMS rats ovarian tissue was upregulated by Exogenous NGF in vitro . (a) Variations of NGF mRNA expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (b) Variations of TrkA mRNA expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (c) Variations of p75 mRNA expression in ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (d) Variations of FSHR mRNA expression in ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . Values are mean ± SD for six samples. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group; # P < 0.05, ## P < 0.01 compared with the NGF group; & P < 0.05, && P < 0.01, compared with the FSH group.

    Journal: BioMed Research International

    Article Title: CUMS Promotes the Development of Premature Ovarian Insufficiency Mediated by Nerve Growth Factor and Its Receptor in Rats

    doi: 10.1155/2020/1946853

    Figure Lengend Snippet: The relative expression of TrkA, p75, and FSHR mRNA of CUMS rats ovarian tissue was upregulated by Exogenous NGF in vitro . (a) Variations of NGF mRNA expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (b) Variations of TrkA mRNA expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (c) Variations of p75 mRNA expression in ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (d) Variations of FSHR mRNA expression in ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . Values are mean ± SD for six samples. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group; # P < 0.05, ## P < 0.01 compared with the NGF group; & P < 0.05, && P < 0.01, compared with the FSH group.

    Article Snippet: A blocking solution was added for incubation at 37°C for 1 h. The following primary antibodies were subsequently used: rabbit polyclonal anti-NGF (1 : 100), mouse monoclonal anti-FSHR (1 : 100; Abcam), rabbit polyclonal anti-TrkA (1 : 100), and mouse monoclonal anti-p75 NGF (1 : 100; Abcam).

    Techniques: Expressing, In Vitro

    The expression of TrkA, p75, and FSHR proteins was upregulated by exogenous NGF in ovarian tissue of CUMS rats in vitro . (a) Variations of NGF protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (b) Variations of TrkA protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (c) Variations of p75 protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (d) Variations of FSHR protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (e) Protein bands for the control, NGF, FSH, and NGF/FSH groups are shown. The molecular weight of TrkA is 150 kDa, FSHR is 77 kDa, p75 is 75 kDa, NGF is 30 kDa, and GAPDH is 38 kDa. Values are mean ± SD for six samples. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group; # P < 0.05, ## P < 0.01 compared with the NGF group; & P < 0.05, && P < 0.01, compared with the FSH group.

    Journal: BioMed Research International

    Article Title: CUMS Promotes the Development of Premature Ovarian Insufficiency Mediated by Nerve Growth Factor and Its Receptor in Rats

    doi: 10.1155/2020/1946853

    Figure Lengend Snippet: The expression of TrkA, p75, and FSHR proteins was upregulated by exogenous NGF in ovarian tissue of CUMS rats in vitro . (a) Variations of NGF protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (b) Variations of TrkA protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (c) Variations of p75 protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (d) Variations of FSHR protein expression in the ovarian tissue of CUMS rats after intervention with exogenous NGF in vitro . (e) Protein bands for the control, NGF, FSH, and NGF/FSH groups are shown. The molecular weight of TrkA is 150 kDa, FSHR is 77 kDa, p75 is 75 kDa, NGF is 30 kDa, and GAPDH is 38 kDa. Values are mean ± SD for six samples. ∗ P < 0.05, ∗∗ P < 0.01, compared with the control group; # P < 0.05, ## P < 0.01 compared with the NGF group; & P < 0.05, && P < 0.01, compared with the FSH group.

    Article Snippet: A blocking solution was added for incubation at 37°C for 1 h. The following primary antibodies were subsequently used: rabbit polyclonal anti-NGF (1 : 100), mouse monoclonal anti-FSHR (1 : 100; Abcam), rabbit polyclonal anti-TrkA (1 : 100), and mouse monoclonal anti-p75 NGF (1 : 100; Abcam).

    Techniques: Expressing, In Vitro, Molecular Weight