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NSDHL (NM_001129765) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC225571L3V
- LentiORF®
-
Lenti ORF particles, NSDHL (Myc-DDK-tagged)-Human NAD(P) dependent steroid dehydrogenase-like (NSDHL), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
| Product Data | |
| Product Name | NSDHL (NM_001129765) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | H105E3; SDR31E1; XAP104 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001129765 |
| ORF Size | 1119 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC225571).
|
| 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_001129765.1, NP_001123237.1 |
| RefSeq Size | 1648 bp |
| RefSeq ORF | 1122 bp |
| Locus ID | 50814 |
| Protein Families | Transmembrane |
| Protein Pathways | Metabolic pathways, Steroid biosynthesis |
| MW | 41.9 kDa |
| Gene Summary | The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008] |
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