XPD (ERCC2) Human shRNA Plasmid Kit (Locus ID 2068)
Specifications
| Product Data | |
| Locus ID | 2068 |
|---|---|
| Synonyms | COFS2; EM9; TFIIH; TTD; TTD1; XPD |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | ERCC2 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 2068). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | NM_000400, NM_001130867, NM_000400.1, NM_000400.2, NM_000400.3, NM_001130867.1, BC008346, BC108255, BC110522, BC110523, BM769772, BM988142, NM_000400.4 |
| UniProt ID | P18074 |
| Summary | 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, Aug 2008 |
| shRNA Design | These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service. |
| Storage | Store at -20°C |
| Shipping | Ambient |
Reviews
Documents
Resources
Citations
Liu, Fang, Chi et al
Nucleic Acids Res. (2015)
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