BD-PT1941

GnRH-R Rabbit Polyclonal Antibody

GNRHR; GRHR; Gonadotropin-releasing hormone receptor; GnRH receptor; GnRH-R

常规抗体

GNRHR

Gonadotropin-releasing hormone receptor

WB

Human,Mouse

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

2798

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2798

P30968

http://www.uniprot.org/uniprotkb/P30968/entry

14715

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=14715

Q01776

http://www.uniprot.org/uniprot/Q01776

The antiserum was produced against synthesized peptide derived from human GNRHR. AA range:41-90

GnRH-R Polyclonal Antibody detects endogenous levels of GnRH-R protein.

WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:5000. Not yet tested in other applications.

37kD

-20°C/1 year

Polyclonal, Rabbit,IgG

This gene encodes the receptor for type 1 gonadotropin-releasing hormone. This receptor is a member of the seven-transmembrane, G-protein coupled receptor (GPCR) family. It is expressed on the surface of pituitary gonadotrope cells as well as lymphocytes, breast, ovary, and prostate. Following binding of gonadotropin-releasing hormone, the receptor associates with G-proteins that activate a phosphatidylinositol-calcium second messenger system. Activation of the receptor ultimately causes the release of gonadotropic luteinizing hormone (LH) and follicle stimulating hormone (FSH). Defects in this gene are a cause of hypogonadotropic hypogonadism (HH). Alternative splicing results in multiple transcript variants encoding different isoforms. More than 18 transcription initiation sites in the 5' region and multiple polyA signals in the 3' region have been identified for this gen

Pituitary, ovary, testis, breast and prostate but not in liver and spleen.

Cell membrane; Multi-pass membrane protein.

Neuroactive ligand-receptor interaction;GnRH;

disease:Defects in GNRHR are a cause of fertile eunuch syndrome [MIM:228300]. Fertile eunuch syndrome is a mild phenotypic form of HH going with the presence of normal testicular size and some degree of spermatogenesis.,disease:Defects in GNRHR are a cause of idiopathic hypogonadotropic hypogonadism (IHH) [MIM:146110]. IHH is defined as a deficiency of the pituitary secretion of follicle-stimulating hormone and luteinizing hormone, which results in the impairment of pubertal maturation and of reproductive function.,function:Receptor for gonadotropin releasing hormone (GnRH) that mediate the action of GnRH to stimulate the secretion of the gonadotropic hormones (LH and FSH). This receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. Isoform 2 may act a an inhibitor of GnRH-R signaling.,similarity:Belongs to the G-protein coupled receptor 1 family.,tissue specificity:Pituitary, ovary, testis, breast and prostate but not in liver and spleen.,

现货

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