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- mouse monoclonal IgG1; 200 µg/ml
- raised against the human B lymphoblast cell line SKW6.4
- recommended for detection of FAS of human origin by WB, IP, IF, IHC(P) and FCM
- fluorescein (sc-21730 FITC) and phycoerythrin (sc-21730 PE) conjugates for FCM, 100 tests
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FAS Background Information Cytotoxic T lymphocyte (CTL)-mediated cytotoxicity constitutes an important component of specific effector mechanisms in immuno-surveillance against virus-infected or transformed cells. Two mechanisms appear to account for this activity, one of which is the perforin-based process. Independently, a FAS-based mechanism involves the transducing molecule FAS (also designated APO-1) and its ligand (FAS-L). The human FAS protein is a cell surface glycoprotein that belongs to a family of receptors that includes CD40, nerve growth factor receptors and tumor necrosis factor receptors. The FAS antigen is expressed on a broad range of lymphoid cell lines, certain of which undergo apoptosis in response to treatment with antibody to FAS. These findings strongly imply that targeted cell death is potentially mediated by the intercellular interactions of FAS with its ligand or effectors, and that FAS may be critically involved in CTL-mediated cytotoxicity. |
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FAS (C236)
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Western blot analysis of FAS expression in A-431 whole cell lysate immunoprecipitated with FAS (C236): sc-21730 and detected with FAS (B-10): sc-8009.
FAS (C236) PE: sc-21730 PE. FCM analysis of MCF7 cells. Black line histogram represents the isotype control, normal mouse IgG 1: sc-2866.
FAS (C236): sc-21730. Western blot analysis of FAS expression in non-transfected: sc-117752 (A) and human FAS transfected: sc-113770 (B) 293T whole cell lysates.
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