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Sterol carrier protein 2 (SCP2) (NM_001193599) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC231295L4V
- LentiORF®
-
Lenti ORF particles, SCP2 (mGFP-tagged)-Human sterol carrier protein 2 (SCP2), transcript variant 7, 200ul, >10^7 TU/mL
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CNY 10,925.00
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CNY 1,999.00
CNY 2,700.00
Specifications
| Product Data | |
| Product Name | Sterol carrier protein 2 (SCP2) (NM_001193599) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | NLTP; NSL-TP; SCOX; SCP-2; SCP-CHI; SCP-X; SCPX |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001193599 |
| ORF Size | 1569 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC231295).
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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_001193599.1 |
| RefSeq ORF | 1572 bp |
| Locus ID | 6342 |
| Protein Pathways | Metabolic pathways, PPAR signaling pathway, Primary bile acid biosynthesis |
| MW | 56.9 kDa |
| Gene Summary | This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer SCPx protein, and the transcript initiated from the distal promoter encodes the shorter SCP2 protein, with the 2 proteins sharing a common C-terminus. Evidence suggests that the SCPx protein is a peroxisome-associated thiolase that is involved in the oxidation of branched chain fatty acids, while the SCP2 protein is thought to be an intracellular lipid transfer protein. This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms.[provided by RefSeq, Aug 2010] |
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