BCR Human shRNA Plasmid Kit (Locus ID 613)
Specifications
| Product Data | |
| Locus ID | 613 |
|---|---|
| Synonyms | ALL; BCR1; CML; D22S11; D22S662; PHL |
| Vector | pRFP-C-RS |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Retroviral plasmids |
| Components | BCR - Human, 4 unique 29mer shRNA constructs in retroviral RFP vector(Gene ID = 613). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRFP-C-RS Vector, TR30015, included for free. |
| RefSeq | NM_004327, NM_021574, NM_004327.1, NM_004327.2, NM_004327.3, NM_021574.1, NM_021574.2, BC031568, BC041705, BC053641, BC063619, BC066122, BC071742, BC083493, BC169208, NM_021574.3, NM_004327.4 |
| UniProt ID | P11274 |
| Summary | A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The unregulated tyrosine kinase activity of BCR-ABL1 contributes to the immortality of leukaemic cells. The BCR protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac and other kinases. Two transcript variants encoding different isoforms have been found for this gene.provided by RefSeq, Jan 2020 |
| 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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