Answers are grounded in this paper and cite their sources.
A sensitive cell surface ELISA is described to detect interleukin-4 (IL-4)-induced major histocompatibility complex class II expression on murine B cells. The ELISA is performed on B cells cultured for 16 h in the presence of purified IL-4 or T cell-derived supernatants. A sandwich technique employing a biotin-conjugated monoclonal anti-I-E antibody followed by avidin-conjugated alkaline phosphatase is used to detect enhanced I-E MHC antigen expression on the B cells. Detection of I-E induced by both purified IL-4 and a T cell-derived supernatant was highly reproducible and sensitive using this method. Other lymphokines were found to be negative for the induction of I-E. The assay is easily performed and many sample supernatants can be rapidly screened for IL-4 activity. In addition, a general method for the removal of endogenous inhibitors of lymphokines from complex supernatants is described.
No takes yet. Share an insight, caveat, or question.
Bartlett et al. (1987) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: