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EHHADH (NM_001966) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC207928L4V
- LentiORF®
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Lenti ORF particles, EHHADH (mGFP-tagged) - Human enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase (EHHADH), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 15,200.00
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CNY 1,999.00
CNY 2,700.00
Specifications
| Product Data | |
| Product Name | EHHADH (NM_001966) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | ECHD; FRTS3; L-PBE; LBFP; LBP; MFE1; PBFE |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001966 |
| ORF Size | 2169 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC207928).
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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_001966.2 |
| RefSeq Size | 3870 bp |
| RefSeq ORF | 2172 bp |
| Locus ID | 1962 |
| Domains | ECH, 3HCDH, 3HCDH_N |
| Protein Pathways | beta-Alanine metabolism, Butanoate metabolism, Fatty acid metabolism, Limonene and pinene degradation, Lysine degradation, Metabolic pathways, PPAR signaling pathway, Propanoate metabolism, Tryptophan metabolism, Valine, leucine and isoleucine degradation |
| MW | 79.5 kDa |
| Gene Summary | The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009] |
Documents
| Product Manuals |
| FAQs |
| SDS |
