Conclusion The GRA7 gene may be expressed as a GST fusion protein in E. coli.
结论GRA7基因在大肠埃希菌中以gst融合蛋白的形式得到表达。
Monoclonal antibody is produced by immunizing animals with a GST fusion protein.
单克隆抗体通过合成GST融合蛋白免疫动物制备。
To investigate the function of PRAK in vivo, a GST fusion protein of PRAK was used as a bait and screened through T7 phage display system.
为了研究PRAK在细胞内的确切功能，我们利用GST-PRAK作为诱饵，通过T7噬菌体展示系统进行了筛选。
Objective: to clone the gene of fructose binding protein BL0033 from Bifidobacterium longum NCC2705, and express and purify fusion protein GST-BL0033 in e.
目的：克隆长双歧杆菌ncc 2705株果糖结合蛋白bl 0033的基因，利用大肠杆菌表达GST -BL 0033融合蛋白并纯化。
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。
Objective To express fusion protein of GST and 1-200 residue region containing PR domain of human RIZ1 protein(GSTPR200 fusion protein).
目的：表达与提纯R IZ1第1个至第200个氨基酸含PR结构域的活性GST融合蛋白质（GST-PR200融合蛋白）。
The solubility of GST-TE2 fusion protein was identified and the result indicated that expressed GST-TE2 protein existed as inclusion bodies.
对表达蛋白的可溶性进行鉴定，结果表明表达产物GST-TE2融合蛋白以包涵体形式存在。
Western blot analysis of the GST-TM fusion protein using sera from subjects with crustacean allergy confirmed that TM is the major allergen of Chinese mitten crab.
通过与甲壳类过敏患者血清的免疫印迹反应，证实融合表达的原肌球蛋白具有过敏原性，表明原肌球蛋白是蟹类的主要过敏原之一。
Western blot analysis of the GST-TM fusion protein using sera from subjects with crustacean allergy confirmed that TM is the major allergen of Chinese mitten crab.
通过与甲壳类过敏患者血清的免疫印迹反应，证实融合表达的原肌球蛋白具有过敏原性，表明原肌球蛋白是蟹类的主要过敏原之一。
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