• Product name
    Anti-FSH Receptor antibody
    See all FSH Receptor primary antibodies
  • Description
    Rabbit polyclonal to FSH Receptor
  • Host species
  • Specificity
    Detects endogenous levels of total FSH Receptor protein.
  • Tested applications
    Suitable for: WB, ELISAmore details
  • Species reactivity
    Reacts with: Human
    Predicted to work with: Mouse, Rat
  • Immunogen

    Synthetic peptide derived from an internal region of human FSH Receptor

  • Positive control
    • Transfected Jurkat and HUVEC cell extracts



Our Abpromise guarantee covers the use of ab75200 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB 1/500 - 1/1000. Predicted molecular weight: 78 kDa.
ELISA 1/5000.


  • Function
    Receptor for follicle-stimulating hormone. The activity of this receptor is mediated by G proteins which activate adenylate cyclase.
  • Tissue specificity
    Sertoli cells and ovarian granulosa cells.
  • Involvement in disease
    Defects in FSHR are a cause of ovarian dysgenesis type 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).
    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 enlargement and capillary leak with fluid sequestration. Pathologic features of this syndrome include the presence of multiple serous and hemorrhagic follicular cysts lined by luteinized cells, a condition called hyperreactio luteinalis.
  • Sequence similarities
    Belongs to the G-protein coupled receptor 1 family. FSH/LSH/TSH subfamily.
    Contains 9 LRR (leucine-rich) repeats.
    Contains 1 LRRNT domain.
  • Post-translational
    N-glycosylated; indirectly required for FSH-binding, possibly via a conformational change that allows high affinity binding of hormone.
  • Cellular localization
    Cell membrane.
  • Information by UniProt
  • Database links
  • Alternative names
    • Follicle stimulating hormone receptor antibody
    • Follicle stimulating hormone receptor isoform 1 antibody
    • Follicle-stimulating hormone receptor antibody
    • Follitropin receptor antibody
    • FSH receptor antibody
    • FSH-R antibody
    • Fshr antibody
    • FSHR_HUMAN antibody
    • FSHRO antibody
    • LGR1 antibody
    • MGC141667 antibody
    • MGC141668 antibody
    • ODG1 antibody
    • ovarian dysgenesis 1 antibody
    see all


  • All lanes : Anti-FSH Receptor antibody (ab75200) at 1/500 dilution

    Lane 1 : Transfected Jurkat cell extract
    Lane 2 : Transfected HUVEC cell extract
    Lane 3 : Transfected Jurkat cell extract with immunising peptide at 10 µg

    Lysates/proteins at 10 µg per lane.

    Predicted band size: 78 kDa
    Observed band size: 78 kDa
    Additional bands at: 85 kDa. We are unsure as to the identity of these extra bands.


This product has been referenced in:
  • Quinn MA  et al. Estrogen Deficiency Promotes Hepatic Steatosis via a Glucocorticoid Receptor-Dependent Mechanism in Mice. Cell Rep 22:2690-2701 (2018). WB ; Mouse . Read more (PubMed: 29514097) »
  • Li X  et al. Follicular Stimulating Hormone Accelerates Atherogenesis by Increasing Endothelial VCAM-1 Expression. Theranostics 7:4671-4688 (2017). Read more (PubMed: 29187895) »

See all 4 Publications for this product

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