KALRN Human shRNA Plasmid Kit (Locus ID 8997)
Specifications
| Product Data | |
| Locus ID | 8997 |
|---|---|
| Synonyms | ARHGEF24; CHD5; CHDS5; DUET; DUO; HAPIP; TRAD |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | KALRN - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 8997). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | NM_001024660, NM_003947, NM_007064, NR_028136, NM_001322988, NM_001322989, NM_001322990, NM_001322991, NM_001322992, NM_001322993, NM_001322994, NM_001322995, NM_001322996, NM_001322997, NM_001322998, NM_001322999, NM_001323000, NM_001323001, NM_001024660.1, NM_001024660.2, NM_001024660.3, NM_001024660.4, NM_003947.1, NM_003947.2, NM_003947.3, NM_003947.4, NM_003947.5, NM_007064.2, NM_007064.3, NM_007064.4, BC026865, BC037924, BC058015, BC166705, BM930007, NM_003947.6, NM_007064.5 |
| UniProt ID | O60229 |
| Summary | Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. 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 |
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