hnRNP A1 (HNRNPA1) Human shRNA Plasmid Kit (Locus ID 3178)

SKU TL312381

HNRNPA1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided

Product Data

• Locus ID: 3178
• Synonyms: ALS19; ALS20; hnRNP-A1; hnRNP A1; HNRPA1; HNRPA1L3; IBMPFD3; UP 1
• Vector: pGFP-C-shLenti
• E. coli Selection: Chloramphenicol (34 ug/ml)
• Format: Lentiviral plasmids
• Components: HNRNPA1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 3178). 5µg purified plasmid DNA per construct; 29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
• RefSeq: NM_002136, NM_031157, NR_135167, NM_002136.1, NM_002136.3, NM_031157.1, NM_031157.2, NM_031157.3, BC009600, BC009600.1, BC002355, BC004945, BC012158, BC020442, BC033714, BC035253, BC052296, BC070315, BC071945, BC073162, BC074502, BC078165, BC103707, BC104236, BC104237, BC121133, NM_002136.4, NM_031157.4
• UniProt ID: P09651
• Summary: This gene encodes a member of a family of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs), which are RNA-binding proteins that associate with pre-mRNAs in the nucleus and influence pre-mRNA processing, as well as other aspects of mRNA metabolism and transport. The protein encoded by this gene is one of the most abundant core proteins of hnRNP complexes and plays a key role in the regulation of alternative splicing. Mutations in this gene have been observed in individuals with amyotrophic lateral sclerosis 20. Multiple alternatively spliced transcript variants have been found. There are numerous pseudogenes of this gene distributed throughout the genome. [provided by RefSeq, Feb 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.
• Shipping: Ambient