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北京柏瑞图科技有限公司
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文献和实验Expression and Preparation of Fusion Proteins from Recombinant gt1.1 Phages
-level expression, the relative stability of β-galactosidase fusion proteins, and simple approaches to purify the fusion proteins. After the desired clone is detected and purified, it is often necessary to obtain preparative amounts of recombinant protein
BAC DNA To shear the large insert insert BAC clone, use the Hydroshear by Genemachines. The settings will vary depending on which orifice you are using, and what size fragments you are trying to generate. New orifices need to be "calibrated
癌 CHMas 肥大细胞白血病 SGC-790 胃腺癌 HEL 红细胞白血病 (Erythroleukemia) BGC-823 低分化胃腺癌 HL-60 原髓细胞白血病 (Promyelocytic lenukemia) MKN-45 低分化胃癌 K562 慢性髓原白血病 (chronic myelogenous leukemia) LoVo 结肠腺癌 Hut-78 皮肤T细胞淋巴瘤 Ls-174-T 结肠腺癌 Hut-102 皮肤
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