Kinase Buffer can be used to assay protein kinase activity.
激酶缓冲液用来分析蛋白激酶的活性。
Peptide and protein can be obtained with high yield in aqueous buffer by coupling unprotected peptide segments without activation by enzymatic or chemical agents.
该方法使用非保护的多肽片段，无需酶或化学活化试剂，在缓冲溶液中能够高产率地获得多肽和蛋白质。
Methods: Based on several reported SDS-PAGE systems for low molecular weight protein, the buffer systems, concentrations of separating gel and stacking gel, electrophoresis procedures were optimized.
方法：比较以往报道的各种低分子量蛋白的电泳分离方法，对电泳缓冲液系统、分离胶和浓缩胶的浓度、电泳程序等进行了优化。
After dissolution of inclusion bodies in binding buffer containing 8m Urea, the fusion protein was purified with metal affinity chromatography column, high purity protein was achieved.
包涵体蛋白经含8m尿素的结合缓冲液溶解后，用金属亲和层析法进行纯化，获得了高纯度的目的蛋白。
After dissolution of inclusion bodies in binding buffer containing 8m Urea, the fusion protein was purified with metal affinity chromatography column, high purity protein was achieved.
包涵体蛋白经含8m尿素的结合缓冲液溶解后，用金属亲和层析法进行纯化，获得了高纯度的目的蛋白。
应用推荐