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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Novel purification system for 6xHis-tagged proteins by magnetic affinity separation
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Novel purification system for 6xHis-tagged proteins by magnetic affinity separation

机译:通过磁亲和力分离用于6xHis标记蛋白的新型纯化系统

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We have developed a novel nickel-silica matrix for the generation of magnetic beads for metal-ion affinity chromatography. In contrast to magnetic Ni-NTA agarose beads, the novel particle type (SiMAC) consists of a magnetic core and a nickel-silica composite matrix with the nickel ions tightly integrated in the silica. This results in a much higher number of chelating groups compared with Ni-NTA agarose beads. With the SiMAC beads, greatly improved purification of histidine-tagged proteins from crude bacterial extracts was achieved. The yield was at least twice as high as with conventional materials, the method is faster, since the coupling step is omitted and there is no need for handling toxic Ni~(2+) salts.
机译:我们已经开发了一种新型的镍-二氧化硅基质,用于生成用于金属离子亲和色谱的磁珠。与磁性Ni-NTA琼脂糖珠相反,新型粒子类型(SiMAC)由磁芯和镍离子复合基体组成,镍离子紧密结合在二氧化硅中。与Ni-NTA琼脂糖珠相比,这导致了更高数量的螯合基团。使用SiMAC珠,可以大大提高了从粗细菌提取物中纯化组氨酸标签的蛋白质的能力。收率至少是传统材料的两倍,该方法更快,因为省去了偶联步骤,并且不需要处理有毒的Ni〜(2+)盐。

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