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The expression product of ScFv was purified through Ni-NTA agarose metal affinity resin column and renatured.

经金属螯合亲和层析柱(Ni-NTA agarose)纯化和凝胶柱上性后,ELISA结果证实其具有良好结合β3抗原性。

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Tigogenin was separated completely from the crude sapogenins by macroporous resin column chromatography,only simple solvent Ilelute was used in the column of the separate process.

用大孔树脂为吸附剂色谱方法过程中仅需要简单溶剂-Ⅱ,单一组剑麻皂甙元占粗皂甙元比率高达70%以上。

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