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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)].
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 TFIIH TFIIH basal transcription factor complex 80 kDa subunit TFIIH p80 TFIIH subunit XPD TTD TTD1 xeroderma pigmentosum complementary group D XPD More... Less...
Ordering Information
Between 710 and 760