PLAGL1 Human shRNA Plasmid Kit (Locus ID 5325)

SKU
TL310381
PLAGL1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
  $1,013.00
In Stock*
Specifications
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 construct
29-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
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