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NXTRACT

NuCLEAR Extraction Kit

For mammalian tissue or cultured cells

Synonym(s):

Nuclear Isolation Kit

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About This Item

NACRES:
NA.56
UNSPSC Code:
41105517
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Quality Level

usage

 kit sufficient for 10 extractions (1 ml packed cell volume),  kit sufficient for 100 extractions (100 μl packed cell volume)

technique(s)

protein extraction: suitable, western blot: suitable

shipped in

dry ice

storage temp.

−20°C

General description

The procedure for the nuclear protein extraction method is to allow cells to swell with hypotonic buffer. The cells are then disrupted, the cytoplasmic fraction is removed, and the nuclear proteins are released from the nuclei by a high salt buffer.

Application

NXTRACT kit was used to study the impact of salt on cardiac differential gene expression and coronary lesion in normotensive mineralocorticoid-treated mice. It was also used to test the therapeutic potential of andrographolide for treating endometriosis.

Other Notes

A number of different procedures in the detailed technical bulletin enable the selection that best fits a particular application. For example, choose between detergent and non-detergent extraction of nuclear protein or between the standard hypotonic lysis buffer for most cell types and isotonic lysis buffer for fragile cells. In addition, the kit provides a procedure for salt reduction from the nuclear extract with dilution buffer. NuCLEAR offers the flexiblity you need for optimal protein extraction. Extracts can be prepared in less than 2 hours and are highly pure since there is little or no cross-contamination between nuclear and cytoplasmic extracts.
Recommended Antibodies for Immunodetection L1293, N2662, AMAB90549
Within this kit is a complete system for preparing nuclear and cytoplasmic protein extracts from mammalian tissue or cultured cells. All reagents necessary for extraction are included.

Legal Information

NuCLEAR is a trademark of Sigma-Aldrich Co. LLC


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Kit Components Also Available Separately

Product No.
Description
SDS & Pricing

  • 3× Dilution and Equilibration Buffer 90 mL
    SDS

  • Protease Inhibitor Cocktail 1 mL
    SDS

signalword

Danger

Storage Class

8A - Combustible corrosive hazardous materials

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

wgk

WGK 3

pictograms

CorrosionEnvironment

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - ED ENV 1 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

Regulatory Information

常规特殊物品
低风险生物材料

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Articles

亚细胞组分离心分离是一种常用技术,广泛适用于多种类型的细胞和组织。由于不同细胞器的大小、形状和密度不同,因此通过离心,可从温和均质的样品中轻松分离和纯化细胞器组分。

Centrifugation separates organelles based on size, shape, and density, facilitating subcellular fractionation across various samples.


K A Lee et al.
Gene analysis techniques, 5(2), 22-31 (1988-03-01)
A convenient and rapid method for preparing soluble extracts from the nuclei of as few as 3 x 10(7) mammalian cells (miniextract procedure) is described. By several criteria, miniextracts are comparable to nuclear extracts prepared from large numbers of cells
Isolation of intact nuclei for nuclear extract preparation from a fragile B-lymphocyte cell line.
R B Dyer et al.
BioTechniques, 19(2), 192-195 (1995-08-01)
Fangyuan Dong et al.
EBioMedicine, 39, 472-483 (2018-12-12)
Accumulating evidence has revealed the pivotal role of epigenetic regulation in the pathogenesis of liver disease. However, the epigenetic mechanism that accounts for hepatic stellate cells (HSCs) activation in liver fibrosis remains largely unknown. Primary HSCs were used to screen



Global Trade Item Number

SKUGTIN
NXTRACT-1KT04061838256133