ERCC8 蛋白
(Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. [provided by RefSeq, Jul 2008].
Recommended next Filters:
7 results
custom-made
ERCC8
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).
ELISA, WB, SDS
custom-made
ERCC8
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).
ELISA, WB, SDS
Aliases for ERCC8 蛋白
excision repair cross-complementation group 8 (ercc8) 蛋白ERCC excision repair 8, CSA ubiquitin ligase complex subunit (ERCC8) 蛋白
ERCC excision repair 8, CSA ubiquitin ligase complex subunit (Ercc8) 蛋白
excision repaiross-complementing rodent repair deficiency, complementation group 8 (Ercc8) 蛋白
2410022P04Rik 蛋白
2810431L23Rik 蛋白
4631412O06Rik 蛋白
B130065P18Rik 蛋白
CKN1 蛋白
Ckn1 蛋白
CSA 蛋白
Csa 蛋白
UVSS2 蛋白
zgc:103550 蛋白
您还需要查找其他产品吗？
You are here:
