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作 者:童铁钢[1] 林燕[1,2] 穆丹梅[3,4] 白宇[1] 杨木蕾[3] 郑敏[3] 吴东来[1]
机构地区:[1]中国农业科学院哈尔滨兽医研究所,农业部兽医公共卫生重点开放实验室,兽医生物技术国家重点实验室,黑龙江哈尔滨150001 [2]黑龙江大学生命科学院,黑龙江哈尔滨150080 [3]哈尔滨医科大学附属第一医院,黑龙江哈尔滨150001 [4]大庆油田总医院腹部超声室,黑龙江大庆163001
出 处:《南方医科大学学报》2009年第6期1094-1097,1110,共5页Journal of Southern Medical University
基 金:黑龙江省自然科学基金重点项目(ZJY-0603-02)
摘 要:目的在大肠杆菌中表达人Id-2与谷胱甘肽-S转移酶(GST)的融合蛋白,并制备抗人Id-2的多克隆抗体。方法从乳腺癌组织中提取总RNA,用RT-PCR扩增出Id-2基因的编码序列,克隆至表达载体pGEX-6P-1中,重组质粒经PCR、酶切、测序鉴定后,在大肠杆菌中经IPTG诱导表达获得GST-Id-2蛋白,SDS-PAGE分析表达产物。通过亲和层析法纯化表达的GST-Id-2融合蛋白,Western-Blot检测重组抗原的免疫原性,并以此为抗原制备多克隆抗体。结果经PCR、酶切、测序鉴定证明,Id-2基因已正确克隆至pGEX-6P-1中,经IPTG诱导后,表达出相对分子质量40000的GST-Id-2融合蛋白。Western-Blot、ELISA和琼脂双向扩散实验鉴定所制备的多克隆抗体可以与GST-Id-2特异性反应。结论Id-2基因在在大肠杆菌中的成功表达及制备的多克隆抗体,为检测Id-2及其在各种组织中的表达提供了一种检测方法,也为分析Id-2分子结构及抗原表位奠定了基础。Objective To express the fusion protein of glutathione S-transferase (GST) and human Id-2 in E. coli and prepare the polyclonal antibodies against Id-2. Methods The coding sequence of Id-2 gene was amplified by RT-PCR from the total RNA of breast cancer tissue. The recombinant plasmid was identified by PCR, restriction endonuclease digestion analysis and sequencing. The fusion protein GST-Id-2 expressed in E coli following IPTG induction was purified by glutathione-agarose affinity chromatography and used to immunize rabbits to prepare the polyclonal antibodies against GST-Id-2. Results PCR, restriction endonuclease digestion and sequence analyses showed that the Id-2 gene had been correctly inserted into pGEX-6P-1 vector, and the GST-Id-2 fusion protein expressed had a relative molecular mass of approximately 40 000 as shown by SDS-PAGE. The polyclonal antibodies obtained from the rabbit sera were found to specifically react with purified Id-2 by Western blotting, ELISA and agar gel immunodiffusion (AGP). Conclusion The prepared polyclonal antibodies against Id-2 allow effective Id-2 detection and facilitate further investigation of the structure and antigen epitope of Id-2.
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