Butyl-agarosechromatography media were prepared by direct coupling of butyl glycidyl ether (BGE) on agarose 4ff beads.
以快流速琼脂糖凝胶为基质，采用直接偶联法制备丁基琼脂糖疏水层析介质。
2
It showed a single spot when identified by means of the paper chromatography, cellulose acetate electrophoresis and agarose electrophoresis.
经纸层析，醋酸纤维素薄膜电泳及琼脂糖电泳分析表明，其主成分为单一斑点。
3
The dsRNA was extracted from RRSV infected rice tissue using CF-11 cellulose column chromatography and further purified through agarose gel electrophoresis.