PLAGL1 Human shRNA Plasmid Kit (Locus ID 5325)
Specifications
| Product Data | |
| Locus ID | 5325 |
|---|---|
| Synonyms | LOT1; ZAC; ZAC1 |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral plasmids |
| Components | PLAGL1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 5325). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
| RefSeq | NM_001080951, NM_001080952, NM_001080953, NM_001080954, NM_001080955, NM_001080956, NM_001289037, NM_001289038, NM_001289039, NM_001289040, NM_001289041, NM_001289042, NM_001289043, NM_001289044, NM_001289045, NM_001289046, NM_001289047, NM_001289048, NM_001289049, NM_001317156, NM_001317157, NM_001317158, NM_001317159, NM_001317160, NM_001317161, NM_001317162, NM_002656, NM_006718, NM_001080954.1, NM_001080954.2, NM_001080955.1, NM_001080955.2, NM_001080952.1, NM_001080952.2, NM_006718.1, NM_006718.2, NM_006718.3, NM_006718.4, NM_001080951.1, NM_001080951.2, NM_001080953.1, NM_001080953.2, NM_001080956.1, NM_001080956.2, NM_001289037.1, NM_001289038.1, NM_001289039.1, NM_001289040.1, NM_001289041.1, NM_001289042.1, NM_001289043.1, NM_001289044.1, NM_001289045.1, NM_001289046.1, NM_001289047.1, NM_001289048.1, NM_001289049.1, NM_002656.2, NM_002656.3, BC109086, BC074814, BC109085, NM_006718.5, NM_001289039.2, NM_001289037.2, NM_001080954.3, NM_001289044.2, NM_001080953.3, NM_001080955.3, NM_001289040.2, NM_001289049.2, NM_001289041.2, NM_001080951.3, NM_001289048.2, NM_001080956.3, NM_001289046.2, NM_001289042.2, NM_001289045.2, NM_001080952.3 |
| UniProt ID | Q9UM63 |
| Summary | This gene encodes a C2H2 zinc finger protein that functions as a suppressor of cell growth. This gene is often deleted or methylated and silenced in cancer cells. In addition, overexpression of this gene during fetal development is thought to be the causal factor for transient neonatal diabetes mellitus (TNDM). Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding two different protein isoforms. The P1 downstream promoter of this gene is imprinted, with preferential expression from the paternal allele in many tissues. provided by RefSeq, Nov 2015 |
| 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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