ABHD11 Human shRNA Plasmid Kit (Locus ID 83451)
Specifications
| Product Data | |
| Locus ID | 83451 |
|---|---|
| Synonyms | abhydrolase domain containing 11; PP1226; WBSCR21; Williams Beuren syndrome chromosome region 21 |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | ABHD11 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 83451). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | NM_001145363, NM_001145364, NM_001301058, NM_001321382, NM_001321383, NM_031295, NM_148912, NM_148913, NM_148914, NM_148915, NM_148916, NR_026910, NR_026912, NR_135627, NM_148912.1, NM_148912.3, NM_001145364.1, NM_001145364.2, NM_148913.1, NM_148913.2, NM_148913.3, NM_001301058.1, NM_001145363.1, NM_148916.3, NM_031295.3, NM_148914.2, NM_148915.2, NM_148916.2, BC008251, BC008251.1, BC011712, BC067750, BM557977 |
| UniProt ID | Q8NFV4 |
| Summary | This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. provided by RefSeq, Mar 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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