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

Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Recombinant Nanobody (SAA2285)
Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Recombinant Nanobody (SAA2285)
가격(USD):
사양:
  • 50ug
  • 100ug
  • 1mg
수량:
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  • 개요

  • 이미지

  • 참고 문헌

  • 데이터시트

  • SDS

개요
카탈로그 번호MA561013
설명
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.
종 반응성Mouse
응용 분야ELISA, IF, FCM
숙주 종Human
클론성Monoclonal
이소타입VHH-hFc
클론 IDSAA2285
타겟 Mu-type opioid receptor, M-OR-1, MOR-1, Mu opiate receptor, Mu opioid receptor, MOP, hMOP, OPRM1
내독소 수준 Please contact with the lab for this information.
순도 >90% as determined by SDS-PAGE.
정제 Protein A/G purified from cell culture supernatant.
등록번호 P42866
형태 Liquid
저장 완충액 0.01M PBS pH 7.4

데이터시트 인쇄본 또는 로트별 COA에 기재된 구체적인 완충액 정보를 참조하세요.

제품 사용 정보
응용 분야 희석
ELISA 1:2000-1:20000
안정성 및 저장 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.
배경

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
참고사항 For research use only.
이미지
  • Anti-Mouse Mu-type opioid receptor/OPRM1/μOR Recombinant Nanobody (SAA2285)

    SDS-PAGE

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

참고 문헌
Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
Enter any 2 of Mass, Concentration, Volume + Molecular Weight to solve for the unknown.
Mass
=
Concentration
×
Volume
Molecular Weight *
g/mol
Formula
C₁ × V₁ = C₂ × V₂
Enter any 3 of the 4 values to solve for the unknown.
Stock Solution
C₁ (Stock Conc.)
×
V₁ (Stock Vol.)
=
Working Solution
C₂ (Working Conc.)
×
V₂ (Working Vol.)
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