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Description
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
Specifications
Specifications
| Antigen | ERCC2 |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 4G2-2A6 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full length recombinant ERCC2. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | ERCC2 |
| Gene Accession No. | BC008346 |
| Gene Alias | COFS2/EM9/MGC102762/MGC126218/MGC126219/TTD/XPD |
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