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Purification and characterization of monoclonal IgG antibodies recognizing Ebola virus glycoprotein

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Fig. 1. Stable transfection of HEK293 cells with pcDNA3-GP and selection of GP-expressing HEK293 cells (A, B), and evaluation of sera ob- ob-tained after GP DNA vaccination for their ability to recognize GP expressed on the cell surface
Table 1. The binding properties of the purified IgG and IgM antibodies from 7 hybridoma clones
Fig. 2. Purification of the IgG antibodies from the five hybridoma clones, and the evaluation of their Ag-specific binding activity
Fig. 3. Evaluation of the five purified IgG antibodies for their binding activity to the native forms of GP expressed on the cell surface
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