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FADD (NM_003824) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC201805L2V
- LentiORF®
-
Lenti ORF particles, FADD (mGFP-tagged) - Human Fas (TNFRSF6)-associated via death domain (FADD), 200ul, >10^7 TU/mL
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CNY 8,360.00
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Specifications
| Product Data | |
| Product Name | FADD (NM_003824) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | GIG3; MORT1 |
| Vector | pLenti-C-mGFP |
| ACCN | NM_003824 |
| ORF Size | 624 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC201805).
|
| 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_003824.2 |
| RefSeq Size | 1855 bp |
| RefSeq ORF | 627 bp |
| Locus ID | 8772 |
| Domains | DEATH, DED |
| Protein Families | Druggable Genome |
| Protein Pathways | Alzheimer's disease, Apoptosis, Pathways in cancer, RIG-I-like receptor signaling pathway, Toll-like receptor signaling pathway |
| MW | 23.3 kDa |
| Gene Summary | The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors. Interaction of this protein with the receptors unmasks the N-terminal effector domain of this protein, which allows it to recruit caspase-8, and thereby activate the cysteine protease cascade. Knockout studies in mice also suggest the importance of this protein in early T cell development. [provided by RefSeq, Jul 2008] |
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