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UQCRB (NM_006294) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC202685L3V
- LentiORF®
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Lenti ORF particles, UQCRB (Myc-DDK tagged) - Human ubiquinol-cytochrome c reductase binding protein (UQCRB), nuclear gene encoding mitochondrial protein, transcript variant 1, 200ul, >10^7 TU/mL
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CNY 7,410.00
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Specifications
| Product Data | |
| Product Name | UQCRB (NM_006294) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | MC3DN3; QCR7; QP-C; QPC; UQBC; UQBP; UQCR6; UQPC |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_006294 |
| ORF Size | 333 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC202685).
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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_006294.2 |
| RefSeq Size | 4839 bp |
| RefSeq ORF | 336 bp |
| Locus ID | 7381 |
| Domains | UCR_14kD |
| Protein Pathways | Alzheimer's disease, Cardiac muscle contraction, Huntington's disease, Metabolic pathways, Oxidative phosphorylation, Parkinson's disease |
| MW | 13.5 kDa |
| Gene Summary | This gene encodes a subunit of the ubiquinol-cytochrome c oxidoreductase complex, which consists of one mitochondrial-encoded and 10 nuclear-encoded subunits. The protein encoded by this gene binds ubiquinone and participates in the transfer of electrons when ubiquinone is bound. This protein plays an important role in hypoxia-induced angiogenesis through mitochondrial reactive oxygen species-mediated signaling. Mutations in this gene are associated with mitochondrial complex III deficiency. Alternatively spliced transcript variants have been found for this gene. Related pseudogenes have been identified on chromosomes 1, 5 and X. [provided by RefSeq, Dec 2011] |
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