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EMP2 (NM_001424) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC201995L3V
- LentiORF®
-
Lenti ORF particles, EMP2 (Myc-DDK tagged) - Human epithelial membrane protein 2 (EMP2), 200ul, >10^7 TU/mL
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CNY 7,410.00
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规格
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Specifications
| Product Data | |
| Product Name | EMP2 (NM_001424) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | XMP |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001424 |
| ORF Size | 501 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC201995).
|
| 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_001424.3 |
| RefSeq Size | 5186 bp |
| RefSeq ORF | 504 bp |
| Locus ID | 2013 |
| Domains | PMP22_Claudin |
| Protein Families | Transmembrane |
| MW | 19.2 kDa |
| Gene Summary | This gene encodes a tetraspan protein of the PMP22/EMP family. The encoded protein regulates cell membrane composition. It has been associated with various functions including endocytosis, cell signaling, cell proliferation, cell migration, cell adhesion, cell death, cholesterol homeostasis, urinary albumin excretion, and embryo implantation. It is known to negatively regulate caveolin-1, a scaffolding protein which is the main component of the caveolae plasma membrane invaginations found in most cell types. Through activation of PTK2 it positively regulates vascular endothelial growth factor A. It also modulates the function of specific integrin isomers in the plasma membrane. Up-regulation of this gene has been linked to cancer progression in multiple different tissues. Mutations in this gene have been associated with nephrotic syndrome type 10 (NPHS10). [provided by RefSeq, Mar 2015] |
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