ERCC8 抗体
(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:
您想试用我们的人工智能搜索吗？
47 results
Latest Publications for our ERCC8 抗体
: "Cumulative defects in DNA repair pathways drive the PARP inhibitor response in high-grade serous epithelial ovarian cancer cell lines." in: Oncotarget, Vol. 8, Issue 25, pp. 40152-40168, (2018) (PubMed).Aliases for ERCC8 抗体
excision repair cross-complementation group 8 (ercc8) 抗体ERCC excision repair 8, CSA ubiquitin ligase complex subunit (ERCC8) 抗体
ERCC excision repair 8, CSA ubiquitin ligase complex subunit (Ercc8) 抗体
excision repaiross-complementing rodent repair deficiency, complementation group 8 (Ercc8) 抗体
2410022P04Rik 抗体
2810431L23Rik 抗体
4631412O06Rik 抗体
B130065P18Rik 抗体
CKN1 抗体
Ckn1 抗体
CSA 抗体
Csa 抗体
UVSS2 抗体
zgc:103550 抗体
您还需要查找其他产品吗？
You are here:
