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MAL (NM_002371) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC201256L2V
- LentiORF®
-
Lenti ORF particles, MAL (mGFP-tagged) - Human mal, T-cell differentiation protein (MAL), transcript variant a, 200ul, >10^7 TU/mL
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CNY 8,360.00
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规格
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Specifications
| Product Data | |
| Product Name | MAL (NM_002371) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | MVP17; VIP17 |
| Vector | pLenti-C-mGFP |
| ACCN | NM_002371 |
| ORF Size | 459 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC201256).
|
| 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_002371.2 |
| RefSeq Size | 1153 bp |
| RefSeq ORF | 462 bp |
| Locus ID | 4118 |
| Protein Families | Transmembrane |
| MW | 16.7 kDa |
| Gene Summary | The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012] |
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