ERCC8 Human shRNA Plasmid Kit (Locus ID 1161)
Specifications
| Product Data | |
| Locus ID | 1161 |
|---|---|
| Synonyms | CKN1; CSA; UVSS2 |
| Vector | pRS |
| E. coli Selection | Ampicillin |
| Mammalian Cell Selection | Puromycin |
| Format | Retroviral plasmids |
| Components | ERCC8 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 1161). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
| RefSeq | BC009793, NM_000082, NM_001007233, NM_001007234, NM_001290285, NM_001007234.1, NM_001007234.2, NM_000082.1, NM_000082.2, NM_000082.3, NM_001290285.1, BC009793.1, NM_001007233.1, BC093802, BC112227, NM_000082.4, NM_001007234.3 |
| UniProt ID | Q13216 |
| Summary | This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. provided by RefSeq, Mar 2014 |
| 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 |
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