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RXFP3 Antibody (C-term) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q9NSD7 |
|---|---|
| Clone Names | 100603077 |
| Gene ID | 51289 |
|---|---|
| Other Names | Relaxin-3 receptor 1, RLN3 receptor 1, G protein-coupled receptor SALPR, G-protein coupled receptor GPCR135, Relaxin family peptide receptor 3, Somatostatin- and angiotensin-like peptide receptor, RXFP3, RLN3R1, SALPR |
| Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
| Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
| Name | RXFP3 |
|---|---|
| Synonyms | GPCR135, RLN3R1, SALPR |
| Function | Receptor for RNL3/relaxin-3. Binding of the ligand inhibit cAMP accumulation. |
| Cellular Location | Cell membrane; Multi-pass membrane protein. |
| Tissue Location | Expressed predominantly in brain regions. Highest expression in substantia nigra and pituitary, followed by hippocampus, spinal cord, amygdala, caudate nucleus and corpus callosum, quite low level in cerebellum. In peripheral tissues, relatively high levels in adrenal glands, low levels in pancreas, salivary gland, placenta, mammary gland and testis |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
RXFP3 is a receptor for RNL3/relaxin-3. Binding of the ligand inhibit cAMP accumulation.
References
Huang, Y.W., et al. Gynecol. Oncol. 117(2):239-247(2010)van der Westhuizen, E.T., et al. Mol. Pharmacol. 77(5):759-772(2010)Hossain, M.A., et al. Chem Biol Drug Des 73(1):46-52(2009)Zhu, J., et al. Eur. J. Pharmacol. 590 (1-3), 43-52 (2008) :Hossain, M.A., et al. J. Biol. Chem. 283(25):17287-17297(2008)
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