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FSHR Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-71795

  • Amount:

    100ul

  • Molecular Weight:

    78295 DaObserved Band:70 KD

  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA

  • Reactivity:

    Human;Mouse;Rat

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human FSHR. AA range:211-260

  • Source:

    Polyclonal, Rabbit,IgG

  • Western Blot analysis of various cells using FSHR Polyclonal Antibody diluted at 1:1000

  • Gene Name:

    FSHR

  • Dilution:

    IHC-p: 100-300.Western Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.

  • Protein Name:

    Follicle-stimulating hormone receptor

  • Human Gene Id:

    2492

  • Human Swiss Prot No:

    P23945

  • Mouse Gene Id:

    14309

  • Mouse Swiss Prot No:

    P35378

  • Rat Gene Id:

    25449

  • Rat Swiss Prot No:

    P20395

  • Specificity:

    FSHR Polyclonal Antibody detects endogenous levels of FSHR protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    FSHR; LGR1; Follicle-stimulating hormone receptor; FSH-R; Follitropin receptor

  • Background:

    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],

  • Function:

    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

  • Subcellular Location:

    Cell membrane ; Multi-pass membrane protein .

  • Expression:

    Sertoli cells and ovarian granulosa cells.

  • Western Blot analysis of KB cells using FSHR Polyclonal Antibody diluted at 1:1000

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Catalog Number

  • Amount:100ul
  • Price:225$

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FSHR Polyclonal Antibody | EnoGene Biotech Co. Ltd