SOD2 Human shRNA Plasmid Kit (Locus ID 6648)
Specifications
| Product Data | |
| Locus ID | 6648 |
|---|---|
| Synonyms | GClnc1; IPO-B; IPOB; Mn-SOD; MNSOD; MVCD6 |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | SOD2 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 6648). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | BC016934, NM_000636, NM_001024465, NM_001024466, NM_001322814, NM_001322815, NM_001322816, NM_001322817, NM_001322819, NM_001322820, NM_000636.1, NM_000636.2, NM_000636.3, NM_001024465.1, NM_001024465.2, NM_001024466.1, NM_001024466.2, BC016934.1, BC012423, BC012423.1, BC001980, BC016015, BC035422, BC041951, BM724413, BM994509, NM_000636.4, NM_001024465.3, NM_001024466.3 |
| UniProt ID | P04179 |
| Summary | This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in this gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. provided by RefSeq, Apr 2016 |
| 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
Su, Su, Setiawan et al
IJMS (2023) 24 (9), 7706 DOI: 10.3390/ijms24097706
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