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Human XPD/ERCC2 Primer Pair

Catalog #: RDP-155 Datasheet / COA / SDS

Discontinued Product

RDP-155 has been discontinued.
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Human XPD/ERCC2 Primer Pair Summary

Specifications

Storage
Store the unopened product at -20 to -70 °C. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Do not use past expiration date.
Species
Human

Product Datasheets

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Product Datasheet
COA

Background: XPD

The XP (Xeroderma Pigmentosum) family is made up of seven genes, XPA-XPG, involved in nucleotide excision repair (ER). Mutations can result in XP, an autosomal recessive genetic disorder characterized by extreme sensitivity to ultraviolet light and a predisposition to skin cancer. XP variant (XPV) is a form of XP caused by mutation in the DNA polymerase eta (POLH) gene.

Long Name
Xeroderma Pigmentosum D
Entrez Gene IDs
2068 (Human); 13871 (Mouse); 308415 (Rat)
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; EC 3.6.1; EC 3.6.4.12; EM9; EM9TFIIH basal transcription factor complex 80 kDa subunit; ERCC2; excision repair cross-complementing rodent repair deficiency, complementationgroup 2; MAG; MGC102762; MGC126218; MGC126219; TFIIH 80 kDa subunit; TFIIH basal transcription factor complex helicase subunit; TFIIH basal transcription factor complex helicase XPD subunit; TTD; xeroderma pigmentosum complementary group D; Xeroderma pigmentosum group D-complementing protein; XPD; XPDC; XPDTFIIH p80

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