DcR1 (TNFRSF10C) (NM_003841) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC221313L2V
- LentiORF®
Lenti ORF particles, TNFRSF10C (mGFP-tagged)-Human tumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain (TNFRSF10C), 200ul, >10^7 TU/mL
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CNY 9,405.00
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Specifications
Product Data | |
Product Name | DcR1 (TNFRSF10C) (NM_003841) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CD263; DCR1; DCR1-TNFR; LIT; TRAIL-R3; TRAILR3; TRID |
Vector | pLenti-C-mGFP |
ACCN | NM_003841 |
ORF Size | 777 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC221313).
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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_003841.2 |
RefSeq Size | 1512 bp |
RefSeq ORF | 780 bp |
Locus ID | 8794 |
Domains | TNFR |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Apoptosis, Cytokine-cytokine receptor interaction, Natural killer cell mediated cytotoxicity |
MW | 27.8 kDa |
Gene Summary | The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008] |
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