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Human OPRM1 Recombinant Protein (N-His-KSI) (HA561012)

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Overview
Catalog No.HA561012
Description
Recombinant Human OPRM1 Protein, N-His-KSI (HA561012) expressed in E. coli. Purity: >90% as determined by SDS-PAGE..
Highlights
  • E. coli Expression — High-yield, cost-effective production.
  • High Purity — >90% as determined by SDS-PAGE.
Expression systemE. coli
AccessionP35372
Protein lengthAsp2-Ile68&Ala339-Pro400
ApplicationsELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
SpeciesHomo sapiens (Human)
Nature Recombinant
Endotoxin level Please contact with the lab for this information.
Purity >90% as determined by SDS-PAGE.
Form Lyophilized
Storage buffer Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Reconstitution Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternate NamesM-OR-1, MOP, MOR-1, MOR1, Mu opiate receptor, Mu opioid receptor, Mu-type opioid receptor, OPRM1, hMOP
Background

Mu-type opioid receptor is a ~44 kDa protein. Receptor for endogenous opioids such as beta-endorphin and endomorphin. Receptor for natural and synthetic opioids including morphine, heroin, DAMGO, fentanyl, etorphine, buprenorphin and methadone. Also activated by enkephalin peptides, such as Met-enkephalin or Met-enkephalin-Arg-Phe, with higher affinity for Met-enkephalin-Arg-Phe. Agonist binding to the receptor induces coupling to an inactive GDP-bound heterotrimeric G-protein complex and subsequent exchange of GDP for GTP in the G-protein alpha subunit leading to dissociation of the G-protein complex with the free GTP-bound G-protein alpha and the G-protein beta-gamma dimer activating downstream cellular effectors. The agonist- and cell type-specific activity is predominantly coupled to pertussis toxin-sensitive G(i) and G(o) G alpha proteins, GNAI1, GNAI2, GNAI3 and GNAO1 isoforms Alpha-1 and Alpha-2, and to a lesser extent to pertussis toxin-insensitive G alpha proteins GNAZ and GNA15.

1. Zhang, P. et al. (1999) Brain research. Molecular brain research 72, 195-204. PMID: 10529478
2. Pan, YX. et al. (2003) Biochemical and biophysical research communications 301, 1057-61. PMID: 12589820
3. Mestek, A. et al. (1995) The Journal of neuroscience : the official journal of the Society for Neuroscience 15, 2396-406. PMID: 7891175
4. Wang, JB. et al. (1994) FEBS letters 338, 217-22. PMID: 7905839
5. Bare, LA. et al. (1994) FEBS letters 354, 213-6. PMID: 7957926
6. Bond, C. et al. (1998) Proceedings of the National Academy of Sciences of the United States of America 95, 9608-13. PMID: 9689128
7. Law, PY. et al. (2000) Annual review of pharmacology and toxicology 40, 389-430. PMID: 10836142
8. Lopez, A. et al. (2009) Cellular and molecular life sciences : CMLS 66, 2093-108. PMID: 19300905
Note For research use only
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Formula
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