XPD Antibody

XPD (Xeroderma pigmentosum group D-complementing protein) is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. XPD has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in the XPD gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome [taken from NCBI Entrez Gene (Gene ID: 2068)].
ERCC2
ERCC excision repair 2, TFIIH core complex helicase subunit
TFIIH basal transcription factor complex helicase XPD subunit
:  basic transcription factor 2 80 kDa subunit BTF2 p80 COFS2 CXPD DNA excision repair protein ERCC-2 DNA repair protein complementing XP-D cells EM9 excision repair cross-complementation group 2 excision repair cross-complementing rodent repair deficiency, complementation group 2 general transcription and DNA repair factor IIH helicase subunit XPD TFIIH TFIIH 80 kDa subunit TFIIH basal transcription factor complex 80 kDa subunit TFIIH basal transcription factor complex helicase subunit TFIIH basal transcription factor complex helicase XPB subunit TFIIH basal transcription factor complex helicase XPD subunit TFIIH p80 TFIIH subunit XPD TTD TTD1 xeroderma pigmentosum complementary group D xeroderma pigmentosum group D-complementing protein XPD More... Less...
Product
Specifications
Ordering Information
Human
WB, IP
Between 710 and 760
$339
$229
$99