跳转至内容
Merck
CN
所有图片(1)

主要文件

MABE1798

Sigma-Aldrich

Anti-ATRX Antibody

mouse monoclonal, 39F

别名:

ATP-dependent helicase ATRX, X-linked helicase II, X-linked nuclear protein, XNP, Znf-HX, EC:3.6.4.12

登录查看公司和协议定价


About This Item

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41

产品名称

Anti-ATRX Antibody, clone 39f, clone 39F, from mouse

生物来源

mouse

质量水平

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

39F, monoclonal

种属反应性

human, mouse

技术

immunocytochemistry: suitable
western blot: suitable

同位素/亚型

IgG1κ

NCBI登记号

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

human ... ATRX(546)

一般描述

Transcriptional regulator ATRX (UniProt: P46100; also known as EC:3.6.4.12, ATP-dependent helicase ATRX, X-linked helicase II, X-linked nuclear protein, XNP, Znf-HX, ATRX) is encoded by the ATRX (also known as RAD54L, XH2) gene (Gene ID: 546) in human. ATRX is ubiquitously distributed and is involved in transcriptional regulation and chromatin remodeling. ATRX has a PHD zinc finger motif and an ATPase/helicase domain of the SWI/SNF type. It facilitates DNA replication in multiple cellular environments and is required for efficient replication of a subset of genomic loci. ATRX binds to DNA tandem repeat sequences in both telomeres and euchromatin and is shown to bind quadruplex structures in vitro. ATRX associates with pericentromeric heterochromatin during interphase and mitosis, probably by interacting with CBX5/HP1 alpha. It interacts with DAXX to form the chromatin remodeling complex ATRX:DAXX, which has ATP-dependent DNA translocase activity and catalyzes the replication-independent deposition of histone H3.3 in pericentric DNA repeats outside S-phase and telomeres. ATRX is believed to be involved in telomere maintenance via recombination in ALT (alternative lengthening of telomeres) cell lines. ATRX is phosphorylated at serine residues during mitosis and phosphorylation is most evident at pro-metaphase stage. Phosphorylation of ATRX is necessary for release of the protein from the nuclear matrix and that it may facilitate progression to mitosis. Dephosphorylation of ATRX seems to coincide with exit of the cells from M phase. Mutations in ATRX gene are known to cause severe psychomotor and mental retardation, facial dysmorphism, and urogenital abnormalities. (Ref.: Berube, NG et al. (2000). Hum. Mol. Gen. 9(4):539-547).

特异性

Clone 39f specifically recognizes human ARTX. This clone binds to an epitope beetween amino acid 85-319 in the N-terminal half of human ATRX.

免疫原

Recombinant fragment corresponding to 235 amino acids from the N-terminal half of human ARTX.

应用

Anti-ATRX Antibody, clone 39f, Cat. No. MABE1798, is a highly specific mouse monoclonal antibody that targets ATRX and has been tested in Immunocytochemistry and Western Blotting .
Immunocytochemistry Analysis: A representative lot detected ATRX in HeLa cells (McDowell, T.L., et. al. (1999). Proc Natl Acad Sci USA. 96(24):13983-8).

Western Blotting Analysis: A representative lot detected ATRX in EBV-transformed lymphocytes (McDowell, T.L., et. al. (1999). Proc Natl Acad Sci USA. 96(24):13983-8).

Western Blotting Analysis: A representative lot detected ATRX in depletion in fibroblasts (Lukashchuk, V., et. al. (2008). J Virol. 82(24):12543-54).

质量

Evaluated by Western Blotting in HEK293 cell lysate.

Western Blotting Analysis: A 1:500 dilution of this antibody detected ATRX in 10 µg of HEK293 cell lysate.


目标描述

~282 kDa observed; 282.59 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

外形

Format: Purified

其他说明

Concentration: Please refer to lot specific datasheet.

未找到合适的产品?  

试试我们的产品选型工具.

储存分类代码

12 - Non Combustible Liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Jennifer Garbarino et al.
Translational oncology, 14(9), 101147-101147 (2021-06-13)
Alpha Thalassemia/Mental Retardation Syndrome X-Linked (ATRX) is mutated frequently in gliomas and represents a potential target for cancer therapies. ATRX is known to function as a histone chaperone that helps incorporate histone variant, H3.3, into the genome. Studies have implicated
Anne-Charlotte Stilp et al.
PLoS pathogens, 18(8), e1010748-e1010748 (2022-08-09)
The chromatin remodeling protein alpha thalassemia/mental retardation syndrome X-linked (ATRX) is a component of promyelocytic leukemia nuclear bodies (PML-NBs) and thereby mediates intrinsic immunity against several viruses including human cytomegalovirus (HCMV). As a consequence, viruses have evolved different mechanisms to

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门