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VDAC3 (NM_001135694) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC227390L4V
- LentiORF®
-
Lenti ORF particles, VDAC3 (mGFP-tagged)-Human voltage-dependent anion channel 3 (VDAC3), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 9,120.00
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Specifications
| Product Data | |
| Product Name | VDAC3 (NM_001135694) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | HD-VDAC3; VDAC-3 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001135694 |
| ORF Size | 852 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC227390).
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| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_001135694.2, NP_001129166.1 |
| RefSeq Size | 1557 bp |
| RefSeq ORF | 855 bp |
| Locus ID | 7419 |
| Protein Families | Druggable Genome, Ion Channels: Other |
| Protein Pathways | Calcium signaling pathway, Huntington's disease, Parkinson's disease |
| MW | 30.8 kDa |
| Gene Summary | This gene encodes a voltage-dependent anion channel (VDAC), and belongs to the mitochondrial porin family. VDACs are small, integral membrane proteins that traverse the outer mitochondrial membrane and conduct ATP and other small metabolites. They are known to bind several kinases of intermediary metabolism, thought to be involved in translocation of adenine nucleotides, and are hypothesized to form part of the mitochondrial permeability transition pore, which results in the release of cytochrome c at the onset of apoptotic cell death. Alternatively transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011] |
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