Rabbit anti-XPD Antibody Affinity Purified
Catalog #
XPD
Human
IP
,WB
Rabbit
Polyclonal
Whole IgG
Between 710 and C-terminus
IgG
Unconjugated
Antigen Affinity Purified
Product Details
Human
Human
2 - 8 °C
1 year from date of receipt
USA
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)].
TFIIH basal transcription factor complex helicase XPD subunit
Alternate Names
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
Applications