DIAPH1 Human shRNA Plasmid Kit (Locus ID 1729)
Specifications
| Product Data | |
| Locus ID | 1729 |
|---|---|
| Synonyms | DFNA1; DIA1; DRF1; hDIA1; LFHL1; SCBMS |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | DIAPH1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 1729). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | NM_001079812, NM_001314007, NM_005219, NM_001079812.1, NM_001079812.2, NM_005219.1, NM_005219.2, NM_005219.3, NM_005219.4, BC117257, BC007411, BC143413, BC143414, NM_005219.5, NM_001079812.3 |
| UniProt ID | O60610 |
| Summary | This gene is a homolog of the Drosophila diaphanous gene, and has been linked to autosomal dominant, fully penetrant, nonsyndromic sensorineural progressive low-frequency hearing loss. Actin polymerization involves proteins known to interact with diaphanous protein in Drosophila and mouse. It has therefore been speculated that this gene may have a role in the regulation of actin polymerization in hair cells of the inner ear. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. provided by RefSeq, Jul 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 |
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