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			96-Well Plate

数量	产品目录编号	订购说明	数量 / 包装	公开价
	48-602MAG	Buffer Detection Kit for Magnetic Beads	1 Kit

371780 Sigma-AldrichGP Antagonist-2A - Calbiochem

The GP Antagonist-2A controls the biological activity of GP. This small molecule/inhibitor is primarily used for Neuroscience applications.

GP Antagonist-2A - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

MSDS
分析证书
参考
Data Sheet

同义词: RPKPQQDWFDWDWM

Primary Target: Inhibits the activation of Gq by M1-muscarinic cholinergic receptors

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概述

Replacement Information

重要规格表

Empirical Formula
C₇₉H₁₀₅N₂₁O₁₃S

价格及供货情况

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Description
Overview	A peptide that selectively inhibits the activation of G_q by M₁-muscarinic cholinergic receptors. Also inhibits activation by cholecystokinin receptor in pancreatic acini at 10 µM. Blocks angiotensin II-stimulated sis-inducing factor and STAT3 tyrosine phosphorylation.
Catalogue Number	371780
Brand Family	Calbiochem®
Synonyms	RPKPQQDWFDWDWM

References
References	Hunt, R.A., et al. 1999. Hypertension 34, 603. Tsunoda Y., et al. 1995. Biochem. Biophys. Res. Commun. 211, 648. Mukai, H., et al. 1992. J. Biol. Chem. 267, 16237.

Product Information
ATP Competitive	N
Form	Lyophilized solid
Formulation	Supplied as a trifluoroacetate salt.
Hill Formula	C₇₉H₁₀₅N₂₁O₁₃S
Chemical formula	C₇₉H₁₀₅N₂₁O₁₃S
Reversible	N
Quality Level	MQ100

Applications

Biological Information
Primary Target	Inhibits the activation of Gq by M1-muscarinic cholinergic receptors
Purity	≥95% by HPLC

Physicochemical Information
Cell permeable	N
Peptide Sequence	H-Arg-Pro-Lys-Pro-Gln-Gln-D-Trp-Phe-D-Trp-D-Trp-Met-NH₂

Dimensions

Materials Information

Toxicological Information

Safety Information according to GHS

Safety Information

Product Usage Statements

Storage and Shipping Information
Ship Code	Ambient Temperature Only
Toxicity	Standard Handling
Storage	-20°C
Do not freeze	Ok to freeze
Special Instructions	Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.

Packaging Information

Transport Information

Supplemental Information

Specifications

Global Trade Item Number
产品目录编号	GTIN
371780-1MGCN	04055977213409

Documentation

GP Antagonist-2A - Calbiochem MSDS

职位
物料安全数据表 (MSDS)

GP Antagonist-2A - Calbiochem 分析证书

标题	批号
371780	输入批号

参考

参考信息概述
Hunt, R.A., et al. 1999. Hypertension 34, 603. Tsunoda Y., et al. 1995. Biochem. Biophys. Res. Commun. 211, 648. Mukai, H., et al. 1992. J. Biol. Chem. 267, 16237.

数据表

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision	13-May-2010 JSW
Synonyms	RPKPQQDWFDWDWM
Description	A peptide that selectively inhibits the activation of G_q by M₁-muscarinic cholinergic receptors. Also inhibits activation by cholecystokinin receptor in pancreatic acini at 10 µM. Blocks angiotensin II-stimulated sis-inducing factor and STAT3 tyrosine phosphorylation.
Form	Lyophilized solid
Formulation	Supplied as a trifluoroacetate salt.
Chemical formula	C₇₉H₁₀₅N₂₁O₁₃S
Peptide Sequence	H-Arg-Pro-Lys-Pro-Gln-Gln-D-Trp-Phe-D-Trp-D-Trp-Met-NH₂
Purity	≥95% by HPLC
Solubility	H₂O (25 mg/ml)
Storage	-20°C
Do Not Freeze	Ok to freeze
Special Instructions	Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
Toxicity	Standard Handling
References	Hunt, R.A., et al. 1999. Hypertension 34, 603. Tsunoda Y., et al. 1995. Biochem. Biophys. Res. Commun. 211, 648. Mukai, H., et al. 1992. J. Biol. Chem. 267, 16237.

种类

Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Neurochemicals > Antagonists > Cholinergic Receptor Antagonists

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