- Tel: 858.663.9055
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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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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.
For a Fas ligand monoclonal with exceptionally strong protein microarray target separation and complementary IHC validation, see our Fas Ligand Antibody FASLG/4455 / CD95L Antibody page.
Optimal dilution of the Fas Ligan Antibody FASLG/4456 / Fas L Monoclonal Antibody should be determined by the researcher.
A portin of amino acids 107-222 from the human protein was used as the immunogen for the Fas Ligan Antibody FASLG/4456.
Aliquot the Fas Ligan Antibody FASLG/4456 and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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