Established an effective in vitro refolding method for single domain antibody inclusion bodies.
Dilution refolding conditions for sdAb specific against human beta-2-microglobulin were optimized.
The antigen-binding activity of refolded sdAb was assayed by ELISA and isothermal titration calorimetry.
Provide an important strategy for the recombinant production and application of sdAb.
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