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TACR1 Antibody (Center) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | P25103 |
|---|---|
| Clone Names | 100430250 |
| Gene ID | 6869 |
|---|---|
| Other Names | Substance-P receptor, SPR, NK-1 receptor, NK-1R, Tachykinin receptor 1, TACR1, NK1R, TAC1R |
| Target/Specificity | The synthetic peptide sequence used to generate the antibody AP13899c was selected from the Center region of TACR1. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
| 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 | TACR1 |
|---|---|
| Synonyms | NK1R, TAC1R |
| Function | This is a receptor for the tachykinin neuropeptide substance P. It is probably associated with G proteins that activate a phosphatidylinositol-calcium second messenger system. The rank order of affinity of this receptor to tachykinins is: substance P > substance K > neuromedin-K. |
| Cellular Location | Cell membrane; Multi-pass membrane protein. |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene belongs to a gene family of tachykininreceptors. These tachykinin receptors are characterized byinteractions with G proteins and contain seven hydrophobictransmembrane regions. This gene encodes the receptor for thetachykinin substance P, also referred to as neurokinin 1. Theencoded protein is also involved in the mediation ofphosphatidylinositol metabolism of substance P. [provided byRefSeq].
References
Saus, E., et al. J Psychiatr Res 44(14):971-978(2010)Pinheiro, A.P., et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 153B (5), 1070-1080 (2010) :Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :Davila, S., et al. Genes Immun. 11(3):232-238(2010)Herlyn, P., et al. Clin J Pain 26(3):175-181(2010)
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