results: ①after the sepharose electrophoresis of rna extracted from rabbit femoral head, the appearances of 5s band, clear 28s and clear 18s suggested that rna was complete.
结果: ①对提取的兔股骨头rna进行琼脂糖凝胶电泳,可显示清晰的28s、18s两个条带,5s条带亦可见,表明了rna是完整的。
the gst-mbd4 fusion protein was purified from cell lysates using glutathione sepharose 4b affinity chromatography.
用谷胱甘肽琼脂糖凝胶4b亲和介质从菌体裂解液中纯化了gst-mbd4融合蛋白。
taking sepharose 4b as carrier, cyanuric chloride as activation reagent, and erythrina trypsin inhibitor as ligand, the method of preparation of affinity chromatography resin is described.
研究用交联琼脂糖为载体,三聚氯氰为活化剂,刺桐胰蛋白酶抑制剂为配基,制备亲和填料的方法。
soil microbial total dna could not be obtained through dna gel extraction kit after purification with 1% sepharose containing 2% of pvp (polyvinylpyrrolidone) agarose gel electrophoresis.
含2 %pvp的1 %琼脂糖凝胶电泳纯化,用dna凝胶回收试剂盒回收后没有得到纯化后的土壤微生物总dna。
the expressed enzyme was purified by means of cell lysis, pei precipitation, heat denaturation, salting out with ammonium sulfate and cm sepharose fast flow chromatography.
表达的酶用聚乙烯亚胺沉淀核酸 ,热变性 ,硫酸铵沉淀 ,层析等方法纯化。
the fraction characteristics of thermo-denatured rice protein(rpi) were analyzed with hplc and sepharose cl-4b gel chromatography and compared with that of natural rice flour glutelin(rfg).
通过色谱法对比分析了热变性米蛋白(rpi)和未加热米蛋白(rfg)的组分特征。
to explore the optimal condition of sepharose activation by means of epichlorohydrin and establish the kinetic model of activation process.
探索环氧氯丙烷法活化琼脂糖凝胶的最佳反应条件,建立活化反应动力学模型。
methods the recombinant protein was extracted by metal chelate sepharose chromatography from e .
方法菌体破碎液经热沉淀处理后,用金属鳌合层析柱纯化重组蛋白。
a comb plate is arranged in the middle groove chamber, sepharose is used to seal the running gel, and macromolecule sample components can be recovered from the running gel.
在中间槽室中配置梳状板并采用琼脂糖凝胶封固电泳凝胶,可以从电泳凝胶中回收大分子样品组分。