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Merck
CN
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文件

安全信息

SRP0406

Sigma-Aldrich

组蛋白 H2a 全长,人

recombinant, expressed in E. coli, ≥90% (SDS-PAGE)

别名:

H2AFQ, histone cluster 2, H2ac

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About This Item

UNSPSC代码:
12352200
NACRES:
NA.32

生物来源

human

重组

expressed in E. coli

检测方案

≥90% (SDS-PAGE)

形式

aqueous solution

分子量

14.8 kDa

包装

pkg of 1 mg

储存条件

avoid repeated freeze/thaw cycles

浓度

1.2 mg/mL

NCBI登记号

UniProt登记号

运输

dry ice

储存温度

−70°C

基因信息

一般描述

Histone cluster 2 H2A family member c (HIST2H2AC) is located on human chromosome 1q21. It is usually present in undifferentiated/proliferating cells. This canonical histone isoform has a protruding tail at both the N- and C-termini.
Histones make up the nucleosome, which is the fundamental unit of the chromatin. Each nucleosome consists of 146 base pairs of DNA which is wrapped around an octamer of four core histones H2A, H2B, H3 and H4. Histone cluster 2 H2A family member c (HIST2H2AC) has many variants. Human Histone 2A (GenBank Accession No. NM_033445) amino acids 2-130 (end) with N-terminal His-tag, MW = 14.8 kDa, expressed in an E. coli expression system.

生化/生理作用

Histone cluster 2 H2A family member c (HIST2H2AC) has a role in maintaining the structure of the chromatin.
Histone cluster 2 H2A family member c (HIST2H2AC) participates in multiple epigenetic regulations and carcinogenesis. It also participates in embryonic stem (ES) cell biology and regulates the expression of genes. It modulates proliferation and epithelial-mesenchymal transition in mammary epithelial and breast cancer cells. Hist2h2ac also controls epithelial differentiation.

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

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The histone H2A isoform Hist2h2ac is a novel regulator of proliferation and epithelial-mesenchymal transition in mammary epithelial and in breast cancer cells
Monteiro FL, et al.
Cancer Letters, 396, 42-52 (2017)
Wenlai Zhou et al.
The international journal of biochemistry & cell biology, 41(1), 12-15 (2008-10-22)
The precise molecular strategies that coordinate patterns of transcriptional response to specific signals is central for understanding normal development and disease. Precise control of transcriptional programs underlying metazoan development is modulated by enzymatically active coregulatory complexes, coupled with epigenetic strategies.
Truncation of histone H2A's C-terminal tail, as is typical for Ni(II)-assisted specific peptide bond hydrolysis, has gene expression altering effects.
Karaczyn AA
Annals of Clinical and Laboratory Science, 39(3), 251-262 (2009)
Acetylation of vertebrate H2A.Z and its effect on the structure of the nucleosome.
Ishibashi T
Biochemistry, 48(22), 5007-5017 (2009)
Rajaganapathi Jagannathan et al.
PloS one, 5(9), e12552-e12552 (2010-09-15)
Chronic activation of angiotensin II (AngII) type 1 receptor (AT(1)R), a prototypical G protein-coupled receptor (GPCR) induces gene regulatory stress which is responsible for phenotypic modulation of target cells. The AT(1)R-selective drugs reverse the gene regulatory stress in various cardiovascular

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