R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
KISS1R (D9D7C) Rabbit mAb #13776
Filter:
- WB
- IP
Supporting Data
REACTIVITY | H |
SENSITIVITY | Endogenous |
MW (kDa) | 40-140 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunoprecipitation | 1:50 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
KISS1R (D9D7C) Rabbit mAb recognizes endogenous levels of total KISS1R protein.
Species Reactivity:
Human
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human KISS1R protein.
Background
The KiSS-1 receptor (KISS1R, GPR54) is a G protein-coupled receptor that inhibits cancer cell metastasis and plays a major role in gonadotropic axis physiology (1). The GPR54 protein was originally described as an orphan receptor homologous to the galanin receptor, and later identified as a receptor for amidated peptide products of the metastasis suppressor gene KiSS-1 (KISS1, Kisspeptin-1) (2,3). In humans, amidated kisspeptin ligands are produced predominantly in cells of the arcuate nucleus and preoptic area, with expression controlled by gonadal hormones (4). Research studies show that deletion of either the KiSS-1 receptor or KiSS-1 gene leads to hypogonadotropic hypogonadism, a disorder characterized by reduced levels of circulating testosterone and gonadotropins, as well as abnormal sexual maturation (5,6). The administration of kisspeptins potently stimulates gonadotropin secretion, indicating that KISS1R and kisspeptins play a major role in the physiology of the gonadotropic axis (7). Additional research demonstrates that KISS1R and kisspeptins inhibit metastasis in cancer cells by inhibiting cell motility (8). However, other studies indicate that increased expression of KISS1R and its ligands in human breast tumors correlates with higher tumor grade and metastatic potential, likely by engaging MMP-9 activation via transactivation of EGFR (9).
- Beck, B.H. and Welch, D.R. (2010) Eur J Cancer 46, 1283-9.
- Lee, D.K. et al. (1999) FEBS Lett 446, 103-7.
- Ohtaki, T. et al. (2001) Nature 411, 613-7.
- Lehman, M.N. et al. (2010) Brain Res 1364, 90-102.
- de Roux, N. et al. (2003) Proc Natl Acad Sci U S A 100, 10972-6.
- d'Anglemont de Tassigny, X. et al. (2007) Proc Natl Acad Sci U S A 104, 10714-9.
- Gottsch, M.L. et al. (2004) Endocrinology 145, 4073-7.
- Cho, S.G. et al. (2012) Cancer Metastasis Rev 31, 585-91.
- Zajac, M. et al. (2011) PLoS One 6, e21599.
限制使用
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For Research Use Only. Not For Use In Diagnostic Procedures.
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