DR4 (TNFRSF10A) Mouse Monoclonal Antibody [Clone ID: OTI8A12]
CAT#: CF807496
Carrier-free (BSA/glycerol-free) TNFRSF10A mouse monoclonal antibody, clone OTI8A12 (formerly 8A12)
Formulation: Standard
Other products for "TNFRSF10A"
Specifications
Product Data | |
Clone Name | OTI8A12 |
Applications | WB |
Recommended Dilution | WB 1:200~2000 |
Reactivities | Human |
Host | Mouse |
Isotype | IgG1 |
Clonality | Monoclonal |
Immunogen | Human recombinant protein fragment corresponding to amino acids 263-468 of human TNFRSF10A(NP_003835) produced in E.coli. |
Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Unconjugated |
Storage | Store at -20°C as received. |
Stability | Stable for 12 months from date of receipt. |
Gene Name | Homo sapiens TNF receptor superfamily member 10a (TNFRSF10A), mRNA. |
Database Link | |
Background | The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL), and thus transduces cell death signal and induces cell apoptosis. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. [provided by RefSeq, Jul 2008] |
Synonyms | APO2; CD261; DR4; TRAILR-1; TRAILR1 |
Reference Data | |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Apoptosis, Cytokine-cytokine receptor interaction, Natural killer cell mediated cytotoxicity |
Documents
Product Manuals |
FAQs |
Resources
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