• Target：
• KiSS-1R

• Fields：
• >>Neuroactive ligand-receptor interaction;>>GnRH secretion

• Gene Name：
• KISS1R

• Protein Name：
• KiSS-1 receptor

• Human Gene Id：
• 84634

• Human Swiss Prot No：
• Q969F8

• Mouse Swiss Prot No：
• Q91V45

• Immunogen：
• The antiserum was produced against synthesized peptide derived from human KISS1R. AA range:301-350

• Specificity：
• KiSS-1R Polyclonal Antibody detects endogenous levels of KiSS-1R protein.

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

• Source：
• Polyclonal, Rabbit,IgG

• Dilution：
• IHC 1:100 - 1:300, IF 1:100 - 1:500. ELISA: 1:5000. Not yet tested in other applications.

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

• Concentration：
• 1 mg/ml

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Other Name：
• KISS1R;AXOR12;GPR54;KiSS-1 receptor;KiSS-1R;G-protein coupled receptor 54;G-protein coupled receptor OT7T175;hOT7T175;Hypogonadotropin-1;Kisspeptins receptor;Metastin receptor

• Molecular Weight(Da)：
• 43kD

• Background：
• The protein encoded by this gene is a galanin-like G protein-coupled receptor that binds metastin, a peptide encoded by the metastasis suppressor gene KISS1. The tissue distribution of the expressed gene suggests that it is involved in the regulation of endocrine function, and this is supported by the finding that this gene appears to play a role in the onset of puberty. Mutations in this gene have been associated with hypogonadotropic hypogonadism and central precocious puberty. [provided by RefSeq, Jul 2008],

• Function：
• disease:Defects in KISS1R are a cause of central precocious puberty [MIM:176400]. Precocious puberty is defined as the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys. Central precocious puberty refers to a gonadotropin-dependent type which results from premature activation of the hypothalamic-pituitary-gonadal axis.,disease:Defects in KISS1R 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 metastin (kisspeptin-54 or kp-54), a C-terminally amidated peptide of KiSS1. KiSS1 is a metastasis suppressor protein that suppresses metastases in malignant melanomas and in some breast carcinomas with

• Subcellular Location：
• Cell membrane; Multi-pass membrane protein.

• Expression：
• Most highly expressed in the pancreas, placenta and spinal cord, with lower-level of expression in peripheral blood leukocytes, kidney, lung, fetal liver, stomach, small intestine, testes, spleen, thymus, adrenal glands and lymph nodes. In the adult brain, expressed in the superior frontal gyrus, putamen, caudate nucleus, cingulate gyrus, nucleus accumbens, hippocampus, pons and amygdala, as well as the hypothalamus and pituitary. Expression levels are higher in early (7-9 weeks) than term placentas. Expression levels were increased in both early placentas and molar pregnancies and were reduced in choriocarcinoma cells. Expressed at higher levels in first trimester trophoblasts than at term of gestation. Also found in the extravillous trophoblast suggesting endocrine/paracrine activation m

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