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Merck
CN
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文件

安全信息

2910

Millipore

Whole Cell Extraction Kit

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About This Item

UNSPSC代码:
41116012
eCl@ss:
32160405

制造商/商品名称

Chemicon®

技术

protein extraction: suitable

应用

sample preparation

运输

dry ice

储存温度

2-8°C

应用

CHEMICON′s Whole Cell Extraction Kit (Catalog No. 2910) provides a simple and convenient method for the preparation of whole cell extractions for use in experimental studies of various cellular proteins.

This kit is recommended for use with CHEMICON′s Rac Activation Assay Kit (Catalog No. SGT425), Cdc42 Activation Assay Kit (Catalog No. SGT430), Ras Activation Assay Kit (Catalog No. SGT435), and CHEMICON′s Transcription Factor Assays when purified nuclear extracts are not required.

For Research Use Only; Not for use in diagnostic procedures
Research Category
All

组分

Whole Cell Extraction Buffer, 5x: - (Part No. 90493) Two vials containing 10 mL of 5x concentrated buffer. Dilute to 1x final concentration with ddH2O prior to use.

Protease Inhibitor Cocktail: - (Part No. 90492) One vial containing 100μL of protease inhibitors in DMSO for use with mammalian cells and tissue extracts. A mixture of protease inhibitors with broad specificity for the inhibition of serine, cysteine, and aspartic acid proteases and aminopeptidases. Contains 4-(2-aminoethyl)benzenesulfonyl fluoride (AEBSF), pepstatin A, E-64, bestatin, leupeptin, and aprotinin. Contains no metal chelators. Prior to use, dilute 1/1000 in 1x Whole Cell Extraction Buffer.

储存及稳定性

· The 5x Whole Cell Extraction Buffer can be stored at 2-8°C until expiration date.

· The prepared 1x Whole Cell Extraction Buffer (with optional additives) should be stored at -20°C for up to one month.

· The undiluted Protease Inhibitor Cocktail can be stored at -20°C until the expiration date.

法律信息

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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.

象形图

CorrosionEnvironment

警示用语:

Danger

危险声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2

储存分类代码

10 - Combustible liquids

法规信息

监管及禁止进口产品

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Yuxuan Xiao et al.
Biochemical and biophysical research communications, 478(2), 919-923 (2016-08-16)
Sumoylation (a covalent modification by Small Ubiquitin-like Modifiers or SUMO proteins) has been implicated in the regulation of various cellular events including cell cycle progression. We have recently identified CDK1, a master regulator of mitosis and meiosis, as a SUMO
Andrew J Schneider et al.
Toxicological sciences : an official journal of the Society of Toxicology, 141(1), 176-187 (2014-06-15)
In utero exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) causes ventral prostate agenesis in C57BL/6J mice by preventing ventral prostatic budding in the embryonic urogenital sinus (UGS). TCDD (5 μg/kg, po) administered to pregnant dams on embryonic day 15.5 (E15.5) activates the aryl
Praveen S Hiremath et al.
AAPS PharmSciTech, 9(4), 1171-1178 (2008-11-19)
The aim of the present investigation was to develop oral controlled release matrix tablet formulations of isoniazid using hydroxypropyl methylcellulose (HPMC) as a hydrophilic release retardant polymer and to study the influence of various formulation factors like proportion of the
Yuxuan Xiao et al.
Reproduction (Cambridge, England), 151(2), 149-166 (2015-12-25)
Recent findings suggest diverse and potentially multiple roles of small ubiquitin-like modifier (SUMO) in testicular function and spermatogenesis. However, SUMO targets remain uncharacterized in the testis due to the complex multicellular nature of testicular tissue, the inability to maintain and
Andrew J Schneider et al.
Gene expression patterns : GEP, 34, 119075-119075 (2019-11-02)
Previous studies identified Sox9 as a critical mediator of prostate development but the precise stage when Sox9 acts had not been determined. A genetic approach was used to delete Sox9 from mouse urogenital sinus epithelium (UGE) prior to prostate specification.

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