MED15 Human shRNA Plasmid Kit (Locus ID 51586)
Specifications
| Product Data | |
| Locus ID | 51586 |
|---|---|
| Synonyms | ARC105; CAG7A; CTG7A; PCQAP; TIG-1; TIG1; TNRC7 |
| Vector | pRS |
| E. coli Selection | Ampicillin |
| Mammalian Cell Selection | Puromycin |
| Format | Retroviral plasmids |
| Components | MED15 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 51586). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
| RefSeq | NM_001003891, NM_001293234, NM_001293235, NM_001293236, NM_001293237, NM_015889, NM_015889.2, NM_015889.3, NM_015889.4, NM_001003891.1, NM_001003891.2, NM_001293236.1, NM_001293235.1, NM_001293237.1, NM_001293234.1, BC013985, BC013985.2, BC003078, BC005027, BC007529, BC017110, NM_001293235.2, NM_001293237.2, NM_001003891.3, NM_015889.5, NM_001293236.2, NM_001293234.2 |
| UniProt ID | Q96RN5 |
| Summary | The protein encoded by this gene is a subunit of the multiprotein complexes PC2 and ARC/DRIP and may function as a transcriptional coactivator in RNA polymerase II transcription. This gene contains stretches of trinucleotide repeats and is located in the chromosome 22 region which is deleted in DiGeorge syndrome. Alternative splicing results in multiple transcript variants. provided by RefSeq, Jun 2014 |
| 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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