ERCC2 抗体
(Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2))
The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008].
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Latest Publications for our ERCC2 抗体
: "Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH." in: Nature genetics, Vol. 20, Issue 2, pp. 184-8, (1998) (PubMed).Aliases for ERCC2 抗体
ERCC excision repair 2, TFIIH core complex helicase subunit (ERCC2) 抗体excision repair cross-complementing rodent repair deficiency, complementation group 2 (Ercc2) 抗体
ERCC excision repair 2, TFIIH core complex helicase subunit (Ercc2) 抗体
excision repair cross-complementation group 2 (ercc2) 抗体
Xeroderma pigmentosum D (Xpd) 抗体
AA407812 抗体
AU020867 抗体
AW240756 抗体
CG9433 抗体
COFS2 抗体
CXPD 抗体
DhR3 抗体
DhXPD 抗体
Dmel\\CG9433 抗体
DmXPD 抗体
EM9 抗体
Ercc-2 抗体
ERCC2 抗体
l(2)SH2 2137 抗体
l(2)SH2137 抗体
MGC89573 抗体
TTD 抗体
XPD 抗体
xpd 抗体
XPD/ERCC2 抗体
zgc:56365 抗体
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