GAA Human shRNA Plasmid Kit (Locus ID 2548)
Specifications
| Product Data | |
| Locus ID | 2548 |
|---|---|
| Synonyms | LYAG |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | GAA - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 2548). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | NM_000152, NM_001079803, NM_001079804, NR_134848, NM_001079804.1, NM_001079804.2, NM_000152.1, NM_000152.2, NM_000152.3, NM_000152.4, NM_001079803.1, NM_001079803.2, BC040431, BC040431.1, BC015908, BC065262, NM_000152.5, NM_001079804.3, NM_001079803.3 |
| UniProt ID | P10253 |
| Summary | This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants. provided by RefSeq, Jan 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 |
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