NT5C3 (NT5C3A) Human shRNA Plasmid Kit (Locus ID 51251)

SKU TL311086

NT5C3A - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided

Product Data

• Locus ID: 51251
• Synonyms: cN-III; hUMP1; NT5C3; P5'N-1; P5N-1; p36; PN-I; POMP; PSN1; UMPH; UMPH1
• Vector: pGFP-C-shLenti
• E. coli Selection: Chloramphenicol (34 ug/ml)
• Format: Lentiviral plasmids
• Components: NT5C3A - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 51251). 5µg purified plasmid DNA per construct; 29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
• RefSeq: NM_001002009, NM_001002010, NM_001166118, NM_016489, NR_029372, NM_001356996, NM_016489.1, NM_016489.10, NM_016489.11, NM_016489.2, NM_016489.3, NM_016489.5, NM_016489.6, NM_016489.7, NM_016489.8, NM_016489.9, NM_001002009.1, NM_001002009.2, NM_001002010.1, NM_001002010.2, NM_001166118.1, NM_001166118.2, BC015856, BC015856.1, BC066914, BC066914.1, BC013292, BC071652, NM_016489.13, NM_001002009.3
• UniProt ID: Q9H0P0
• Summary: This gene encodes a member of the 5'-nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5'-monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5' nucleotidase and catalyzes the dephosphorylation of pyrimidine 5' monophosphates. Mutations in this gene are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and pseudogenes of this gene are located on the long arm of chromosomes 3 and 4. [provided by RefSeq, Mar 2012]
• 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.
• Shipping: Ambient