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TFII I (GTF2I) Human shRNA Plasmid Kit (Locus ID 2969)

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TG304176
GTF2I - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector, 5µg of each construct provided
In Control Promo
  $883.00
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Other products for "TFII I or NM_001163636"

Specifications
Specifications
Product Data
Locus ID 2969
Synonyms BAP135; BTKAP1; DIWS; GTFII-I; IB291; SPIN; TFII-I; WBS; WBSCR6
Vector pGFP-V-RS
E. coli Selection Kanamycin
Mammalian Cell Selection Puromycin
Format Retroviral plasmids
Components GTF2I - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 2969). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free.
RefSeq NM_001163636, NM_001280800, NM_001518, NM_032999, NM_033000, NM_033001, NM_033003, NM_001518.1, NM_001518.2, NM_001518.3, NM_001518.4, NM_033001.1, NM_033001.2, NM_033001.3, NM_032999.1, NM_032999.2, NM_032999.3, NM_033000.1, NM_033000.2, NM_033000.3, NM_001163636.1, NM_001163636.2, NM_001280800.1, BC070484, BC070484.1, BC099907, BC099907.1, BC004472, NM_001163636.3
UniProt ID P78347
Summary This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. provided by RefSeq, Jul 2013
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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