FSHR Polyclonal Antibody

    • 货号:YT1795
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Mouse;Rat
      • 靶点:
      • FSHR
      • 简介:
      • >>cAMP signaling pathway;>>Neuroactive ligand-receptor interaction;>>Ovarian steroidogenesis
      • 基因名称:
      • FSHR
      • 蛋白名称:
      • Follicle-stimulating hormone receptor
      • Human Gene Id:
      • 2492
      • Human Swiss Prot No:
      • P23945
      • Mouse Swiss Prot No:
      • P35378
      • 免疫原:
      • The antiserum was produced against synthesized peptide derived from human FSHR. AA range:211-260
      • 特异性:
      • FSHR Polyclonal Antibody detects endogenous levels of FSHR protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • IHC: 100-300.WB 1:500 - 1:2000. ELISA: 1:5000.. IF 1:50-200
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • FSHR;LGR1;Follicle-stimulating hormone receptor;FSH-R;Follitropin receptor
      • 实测条带:
      • 70kD
      • 背景:
      • The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010],
      • 功能:
      • disease:Defects in FSHR are a cause of ovarian dysgenesis 1 (ODG1) [MIM:233300]; also known as premature ovarian failure or gonadal dysgenesis XX type or XX gonadal dysgenesis (XXGD) or hereditary hypergonadotropic ovarian failure or hypergonadotropic ovarian dysgenesis with normal karyotype. ODG1 is an autosomal recessive disease characterized by primary amenorrhea, variable development of secondary sex characteristics, and high serum levels of follicle-stimulating hormone (FSH) and luteinizing hormone (LH).,disease:Defects in FSHR are a cause of ovarian hyperstimulation syndrome (OHSS) [MIM:608115]. OHSS is a disorder which occurs either spontaneously or most often as an iatrogenic complication of ovarian stimulation treatments for in vitro fertilization. The clinical manifestations vary from abdominal distention and discomfort to potentially life-threatening, massive ovarian enlargeme
      • 细胞定位:
      • Cell membrane ; Multi-pass membrane protein .
      • 组织表达:
      • Sertoli cells and ovarian granulosa cells.

      Ginsenoside Rg1 improves fertility and reduces ovarian pathological damages in premature ovarian failure model of mice:. EXPERIMENTAL BIOLOGY AND MEDICINE Exp Biol Med. 2017;242(7):683-691 WB,IHC Mouse 1:100 ovaries
      货号:YT1795

      • 产品图片
      • Western Blot analysis of various cells using FSHR Polyclonal Antibody diluted at 1:1000
      • Western Blot analysis of KB cells using FSHR Polyclonal Antibody diluted at 1:1000
      • Immunohistochemical analysis of paraffin-embedded Human Amygdala. 1, Antibody was diluted at 1:100(4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).
      • Western blot analysis of lysates from Jurkat and HUVEC cells, using FSHR Antibody. The lane on the right is blocked with the synthesized peptide.