Description
Product Characteristics:
Aliases: TFIIH 80 kDa subunit antibody, Basic transcription factor 2 80 kDa subunit antibody, BTF2 p80 antibody, COFS 2 antibody, COFS2 antibody, CXPD antibody, DNA excision repair protein ERCC 2 antibody, DNA excision repair protein ERCC-2 antibody, DNA repair protein complementing XP D cells antibody, DNA repair protein complementing XP-D cells antibody, EM9 antibody, ERCC 2 antibody, ERCC2 antibody, ERCC2_HUMAN antibody, Excision repair 2 antibody, Excision repair cross complementing rodent repair deficiency complementation antibody, Excision repair cross complementing rodent repair deficiency, complementation group 2 antibody, MAG antibody, MGC102762 antibody, MGC126218 antibody, MGC126219 antibody, OTTHUMP00000045860 antibody, OTTHUMP00000045861 antibody, OTTHUMP00000045862 antibody, OTTHUMP00000045863 antibody, TFIIH 80 kDa subunit antibody, TFIIH basal transcription factor complex 80 kDa subunit antibody, TFIIH Basal Transcription Factor Complex Helicase Subunit antibody, TFIIH basal transcription factor complex helicase XPD subunit antibody, TFIIH basal transcription factor complex p80 subunit antibody, TFIIH p80 antibody, TTD antibody, Xeroderma pigmentosum complementary group D antibody, Xeroderma pigmentosum group D complementing protein antibody, Xeroderma pigmentosum group D-complementing protein antibody, XPD antibody, XPDC antibody
Target Information: 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]