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Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Nanobody (SAA2285) (MA561013)

Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Nanobody (SAA2285)
Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Nanobody (SAA2285)
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  • 50ug
  • 100ug
  • 1mg
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Overview
Catalog No.MA561013
Description
Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Nanobody (SAA2285) [SAA2285] (MA561013) is a human monoclonal antibody detecting Mu-type opioid receptor in ELISA, IF, FCM. Suitable for Mouse.
Highlights
  • Multi-Application — Validated across multiple applications.
  • Flow Cytometry — Validated for flow cytometry applications.
Species reactivityMouse
ApplicationsELISA, IF, FCM
Host speciesHuman
IsotypeVHH-hFc
Clone IDSAA2285
Clonality Monoclonal
Target Mu-type opioid receptor, M-OR-1, MOR-1, Mu opiate receptor, Mu opioid receptor, MOP, hMOP, OPRM1
Endotoxin level Please contact with the lab for this information.
Purity >90% as determined by SDS-PAGE.
Purification Protein A/G purified from cell culture supernatant.
Accession P42866
Form Liquid
Storage buffer 0.01M PBS, pH 7.4.

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

Product Usage Information
Application Dilution
ELISA 1:2000-1:20000
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.
Background

Mu-type opioid receptor (OPRM1/μOR) 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. George, SR. et al. (2000) The Journal of biological chemistry 275, 26128-35. PMID: 10842167
2. Rios, C. et al. (2006) British journal of pharmacology 148, 387-95. PMID: 16682964
3. Milan-Lobo, L. et al. (2011) The Journal of pharmacology and experimental therapeutics 337, 868-75. PMID: 21422164
4. Manglik, A. et al. (2012) Nature 485, 321-6. PMID: 22437502
5. Huang, W. et al. (2015) Nature 524, 315-21. PMID: 26245379
6. Kaufman, DL. et al. (1995) The Journal of biological chemistry 270, 15877-83. PMID: 7797593
7. Sora, I. et al. (1997) Proceedings of the National Academy of Sciences of the United States of America 94, 1544-9. PMID: 9037090
8. Trieu, BH. et al. (2022) Science (New York, N.Y.) 375, 1177-1182. PMID: 35201898
Note For research use only.
Images
  • Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Nanobody (SAA2285)

    SDS-PAGE

    SDS-PAGE for Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Nanobody (SAA2285)

References
Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
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