SLC26A4 Human shRNA Plasmid Kit (Locus ID 5172)
Specifications
| Product Data | |
| Locus ID | 5172 |
|---|---|
| Synonyms | DFNB4; EVA; PDS; TDH2B |
| Vector | pRS |
| E. coli Selection | Ampicillin |
| Mammalian Cell Selection | Puromycin |
| Format | Retroviral plasmids |
| Components | SLC26A4 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 5172). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
| RefSeq | NM_000441, NM_000441.1, BC148375, BC153002, NM_000441.2 |
| UniProt ID | O43511 |
| Summary | Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. 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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