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WASP (WAS) (NM_000377) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC203457L3V
- LentiORF®
-
Lenti ORF particles, WAS (Myc-DDK tagged) - Human Wiskott-Aldrich syndrome (eczema-thrombocytopenia) (WAS), 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
| Product Data | |
| Product Name | WASP (WAS) (NM_000377) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | IMD2; SCNX; THC; THC1; WASP; WASPA |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_000377 |
| ORF Size | 1506 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC203457).
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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_000377.1 |
| RefSeq Size | 1806 bp |
| RefSeq ORF | 1509 bp |
| Locus ID | 7454 |
| Domains | PBD, WH1, WH2 |
| Protein Families | Druggable Genome |
| Protein Pathways | Adherens junction, Chemokine signaling pathway, Fc gamma R-mediated phagocytosis, Pathogenic Escherichia coli infection, Regulation of actin cytoskeleton |
| MW | 52.7 kDa |
| Gene Summary | The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. Wiskott-Aldrich syndrome is a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocytopenia, and is caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in WAS patients. A transcript variant arising as a result of alternative promoter usage, and containing a different 5' UTR sequence, has been described, however, its full-length nature is not known. [provided by RefSeq, Jul 2008] |
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