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Merck
CN

M9558

Sigma-Aldrich

Anti-Muscarinic Acetylcholine Receptor (M2) antibody produced in rabbit

affinity isolated antibody

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About This Item

MDL编号:
UNSPSC代码:
12352203

生物来源

rabbit

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

种属反应性

mouse, human, rat

技术

immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
immunoprecipitation (IP): suitable
western blot (chemiluminescent): 1:200 using brain membranes

UniProt登记号

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... CHRM2(1129)
mouse ... Chrm2(243764)
rat ... Chrm2(81645)

一般描述

Muscarinic acetylcholine receptor M2 is expressed in the heart and many other tissues. The gene encoding it is localized on human chromosome 7.

免疫原

GST fusion protein of a part of the i3 intracellular loop of human M2 muscarinic acetylcholine receptor (mAChR) corresponding to amino acid residues 227-356.1, 2

生化/生理作用

Muscarinic acetylcholine receptor M2 plays an important role in regulating functions of the heart and activities like pain perception and cognition. It is regarded as a good model in GPCR (G protein-coupled receptor) biology pharmacological studies. This receptor has a function in airway remodeling and it enhances the proliferation of airway smooth muscle cells (ASM) which is induced by transforming growth factor-β (TGF-β).

外形

Lyophilized at ~0.3 mg/ml from a solution of phosphate-buffered saline, pH 7.4, containing 1% bovine serum albumin, and 0.05% sodium azide.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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象形图

Skull and crossbonesEnvironment

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品
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分析证书(COA)

Lot/Batch Number

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访问文档库

Matthew R Stoyek et al.
American journal of physiology. Heart and circulatory physiology, 311(3), H676-H688 (2016-06-28)
The cardiac pacemaker sets the heart's primary rate, with pacemaker discharge controlled by the autonomic nervous system through intracardiac ganglia. A fundamental issue in understanding the relationship between neural activity and cardiac chronotropy is the identification of neuronal populations that
Becky J Proskocil et al.
PloS one, 5(5), e10562-e10562 (2010-05-19)
Epidemiological studies link organophosphorus pesticide (OP) exposures to asthma, and we have shown that the OPs chlorpyrifos, diazinon and parathion cause airway hyperreactivity in guinea pigs 24 hr after a single subcutaneous injection. OP-induced airway hyperreactivity involves M2 muscarinic receptor
Andrew C Kruse et al.
Nature, 504(7478), 101-106 (2013-11-22)
Despite recent advances in crystallography and the availability of G-protein-coupled receptor (GPCR) structures, little is known about the mechanism of their activation process, as only the β2 adrenergic receptor (β2AR) and rhodopsin have been crystallized in fully active conformations. Here
Yinglong Miao et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(27), 10982-10987 (2013-06-20)
G-protein-coupled receptors (GPCRs) mediate cellular responses to various hormones and neurotransmitters and are important targets for treating a wide spectrum of diseases. Although significant advances have been made in structural studies of GPCRs, details of their activation mechanism remain unclear.
Deeptankar DeMazumder et al.
Circulation research, 116(10), 1691-1699 (2015-03-04)
Cardiac resynchronization therapy (CRT) is the only heart failure (HF) therapy documented to improve left ventricular function and reduce mortality. The underlying mechanisms are incompletely understood. Although β-adrenergic signaling has been studied extensively, the effect of CRT on cholinergic signaling

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