Nibrin 蛋白
(Nibrin (NBN))
Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. [provided by RefSeq, Jul 2008].
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NBN
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
> 95 %
WB, SDS, Imm, PC
NBN
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
> 95 %
WB, SDS, Imm, PC
custom-made
NBN
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
WB, SDS, ELISA
custom-made
NBN
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
WB, SDS, ELISA
Aliases for Nibrin 蛋白
nibrin (NBN) 蛋白nibrin (nbn) 蛋白
nibrin (Nbn) 蛋白
AT-V1 蛋白
AT-V2 蛋白
ATV 蛋白
im:6911679 蛋白
NBN 蛋白
NBS 蛋白
NBS1 蛋白
Nbs1 蛋白
P95 蛋白
zgc:194152 蛋白
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