重组人 BRCA2 蛋白 (GST tag N-Terminus)
Recombinant Human BRCA2 protein (GST tag N-Terminus)
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(1 Publication)
Recombinant Human BRCA2 protein (GST tag N-Terminus) is a Human Fragment protein, in the 3319 to 3418 aa range, expressed in Wheat germ, suitable for SDS-PAGE, ELISA, WB.
查看别名
FACD, FANCD1, BRCA2, Breast cancer type 2 susceptibility protein, Fanconi anemia group D1 protein
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human BRCA2 protein (GST tag N-Terminus) (AB112253)
Coomassie blue stained 12.5% SDS page analysis of ab112253
反应性数据
序列信息
性能和储存信息
运输条件
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
特殊说明
形式
Liquid
常规信息
功能
Involved in double-strand break repair and/or homologous recombination. Binds RAD51 and potentiates recombinational DNA repair by promoting assembly of RAD51 onto single-stranded DNA (ssDNA). Acts by targeting RAD51 to ssDNA over double-stranded DNA, enabling RAD51 to displace replication protein-A (RPA) from ssDNA and stabilizing RAD51-ssDNA filaments by blocking ATP hydrolysis. Part of a PALB2-scaffolded HR complex containing RAD51C and which is thought to play a role in DNA repair by HR. May participate in S phase checkpoint activation. Binds selectively to ssDNA, and to ssDNA in tailed duplexes and replication fork structures. May play a role in the extension step after strand invasion at replication-dependent DNA double-strand breaks; together with PALB2 is involved in both POLH localization at collapsed replication forks and DNA polymerization activity. In concert with NPM1, regulates centrosome duplication. Interacts with the TREX-2 complex (transcription and export complex 2) subunits PCID2 and SEM1, and is required to prevent R-loop-associated DNA damage and thus transcription-associated genomic instability. Silencing of BRCA2 promotes R-loop accumulation at actively transcribed genes in replicating and non-replicating cells, suggesting that BRCA2 mediates the control of R-loop associated genomic instability, independently of its known role in homologous recombination (PubMed : 24896180).
翻译后修饰
Phosphorylated by ATM upon irradiation-induced DNA damage. Phosphorylation by CHEK1 and CHEK2 regulates interaction with RAD51. Phosphorylation at Ser-3291 by CDK1 and CDK2 is low in S phase when recombination is active, but increases as cells progress towards mitosis; this phosphorylation prevents homologous recombination-dependent repair during S phase and G2 by inhibiting RAD51 binding.. Ubiquitinated in the absence of DNA damage; this does not lead to proteasomal degradation. In contrast, ubiquitination in response to DNA damage leads to proteasomal degradation.
亚细胞定位
Nucleus
靶点信息
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
Biomicrofluidics 12:054108 PubMed30344835
2018
Applications
Unspecified application
Species
Unspecified reactive species
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