HAX1 Human shRNA Plasmid Kit (Locus ID 10456)
Specifications
| Product Data | |
| Locus ID | 10456 |
|---|---|
| Synonyms | HCLSBP1; HS1BP1; SCN3 |
| Vector | pRFP-C-RS |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Retroviral plasmids |
| Components | HAX1 - Human, 4 unique 29mer shRNA constructs in retroviral RFP vector(Gene ID = 10456). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRFP-C-RS Vector, TR30015, included for free. |
| RefSeq | NM_001018837, NM_006118, NM_006118.1, NM_006118.2, NM_006118.3, NM_001018837.1, BC005240, BC005240.1, BC014314, BC015209, BC016730, NM_001018837.2, NM_006118.4 |
| UniProt ID | O00165 |
| Summary | The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different 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 |
Reviews
Documents
Resources
Citations
Gomathinayagam, Muralidharan, Ha et al
Genes Cancer (2014) 5 (3-4), 84-99
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