Bcl x (BCL2L1) Human shRNA Plasmid Kit (Locus ID 598)
Specifications
| Product Data | |
| Locus ID | 598 |
|---|---|
| Synonyms | Bcl-X; BCL-XL/S; BCL2L; BCLX; PPP1R52 |
| Vector | pRS |
| E. coli Selection | Ampicillin |
| Mammalian Cell Selection | Puromycin |
| Format | Retroviral plasmids |
| Components | BCL2L1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 598). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
| RefSeq | NM_001191, NM_001317919, NM_001317920, NM_001317921, NM_001322239, NM_001322240, NM_001322242, NM_138578, NR_134257, NM_138578.1, NM_138578.2, NM_001191.1, NM_001191.2, NM_001191.3, BC019307, BC019307.1, BM554265, NM_001191.4, NM_138578.3 |
| UniProt ID | Q07817 |
| Summary | The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The proteins encoded by this gene are located at the outer mitochondrial membrane, and have been shown to regulate outer mitochondrial membrane channel (VDAC) opening. VDAC regulates mitochondrial membrane potential, and thus controls the production of reactive oxygen species and release of cytochrome C by mitochondria, both of which are the potent inducers of cell apoptosis. Alternative splicing results in multiple transcript variants encoding two different isoforms. The longer isoform acts as an apoptotic inhibitor and the shorter isoform acts as an apoptotic activator. provided by RefSeq, Dec 2015 |
| 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 |
Reviews
Documents
Resources
Citations
Shukla, Tyagi, Chandrasekaran et al
Sci Adv (2025) 11 (24), eadv8640 DOI: 10.1126/sciadv.adv8640
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