PMS1 Human shRNA Plasmid Kit (Locus ID 5378)
Specifications
| Product Data | |
| Locus ID | 5378 |
|---|---|
| Synonyms | HNPCC3; hPMS1; MLH2; PMSL1 |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | PMS1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 5378). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | BC008410, NM_000534, NM_001128143, NM_001128144, NM_001289408, NM_001289409, NR_110332, NM_001321044, NM_001321045, NM_001321046, NM_001321047, NM_001321048, NM_001321049, NM_001321051, NM_000534.1, NM_000534.2, NM_000534.3, NM_000534.4, NM_001128144.1, NM_001128143.1, NM_001289408.1, NM_001289409.1, BC036376, BC084548, BC096330, BC096331, BC096332, BM553209, BM677668, BM800196, NM_001128144.2, NM_001128143.2, NM_000534.5 |
| UniProt ID | P54277 |
| Summary | This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. 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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