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. Author manuscript; available in PMC: 2011 Jun 30.
Published in final edited form as: J Immunol Methods. 2010 Apr 9;358(1-2):104–110. doi: 10.1016/j.jim.2010.04.003

Fig. 2.

Fig. 2

Fig. 2a. Competition ELISA determined binding properties of MIG recognizing purified monoclonal phage-scFv clones selected from Tomlinson I library. MIG analyte concentrations used in biopanning were 5 nM (I5-2, I5-4) and 50 nM (I50-5, I50-11). The data represent mean ± standard deviation from duplicate measurements.

Fig. 2b. Competition ELISA determined binding properties of MIG recognizing purified monoclonal phage-scFv clones selected from Tomlinson J library. MIG analyte concentrations used in biopanning were 5 nM (J5-14, J5-20) and 50 nM (J50-4, J50-6, J50-10, J50-21). The data represent mean ± standard deviation from duplicate measurements.