CHRM1 Antibody (C-term)
Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application ![]()
| WB, E |
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Primary Accession | P11229 |
Reactivity | Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 51421 Da |
Gene ID | 1128 |
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Other Names | Muscarinic acetylcholine receptor M1, CHRM1 |
Target/Specificity | This CHRM1 antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 331-367 amino acids from the C-terminal region of human CHRM1. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | CHRM1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | CHRM1 |
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Function | The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. |
Cellular Location | Cell membrane; Multi-pass membrane protein. Postsynaptic cell membrane; Multi-pass membrane protein |

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Provided below are standard protocols that you may find useful for product applications.
Background
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover.
References
Allard W.J.,et al.Nucleic Acids Res. 15:10604-10604(1987).
Chapman C.G.,et al.Nucleic Acids Res. 18:2191-2191(1990).
Peralta E.G.,et al.EMBO J. 6:3923-3929(1987).
Puhl H.L. III,et al.Submitted (APR-2002) to the EMBL/GenBank/DDBJ databases.
Arden J.R.,et al.Biochem. Biophys. Res. Commun. 188:1111-1115(1992).

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