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HADHB (NM_000183) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC209853L3V
- LentiORF®
-
Lenti ORF particles, HADHB (Myc-DDK tagged) - Human hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit (HADHB), nuclear gene encoding mitochondrial pr, 200ul, >10^7 TU/mL
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Specifications
| Product Data | |
| Product Name | HADHB (NM_000183) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | ECHB; MSTP029; MTPB; TP-BETA |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_000183 |
| ORF Size | 1428 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC209853).
|
| 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_000183.2 |
| RefSeq Size | 2196 bp |
| RefSeq ORF | 1425 bp |
| Locus ID | 3032 |
| Domains | thiolase |
| Protein Pathways | Fatty acid elongation in mitochondria, Fatty acid metabolism, Metabolic pathways, Valine, leucine and isoleucine degradation |
| MW | 51.4 kDa |
| Gene Summary | This gene encodes the beta subunit of the mitochondrial trifunctional protein, which catalyzes the last three steps of mitochondrial beta-oxidation of long chain fatty acids. The mitochondrial membrane-bound heterocomplex is composed of four alpha and four beta subunits, with the beta subunit catalyzing the 3-ketoacyl-CoA thiolase activity. The encoded protein can also bind RNA and decreases the stability of some mRNAs. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head orientation. Mutations in this gene result in trifunctional protein deficiency. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013] |
Documents
| Product Manuals |
| FAQs |
| SDS |
