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作 者:梁勤东[1] 郭变琴[1] 汪仙桃[1] 李武县[1] 董晋豫[1] 王秦[1] 涂植光[1]
机构地区:[1]重庆医科大学检验医学院、重庆医科大学临床检验诊断学教育部重点实验室,重庆400016
出 处:《细胞与分子免疫学杂志》2012年第11期1154-1157,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:国家自然科学基金(81172016)
摘 要:目的:建立CA125串联重复序列(CA125R)原核表达系统,表达纯化重组CA125R蛋白并制备其抗血清。方法:全基因合成一段CA125串联重复序列,并将其克隆至pET-32a(+),构建CA125R蛋白原核表达载体pET-CA125R;将构建好的pET-CA125R载体转化至E.coli BL21(DE3),确定最佳可溶性表达条件,通过Ni-NTA亲和层析系统纯化重组CA125R蛋白;纯化重组蛋白经Western blot方法验证后,免疫家兔制备抗血清。结果:成功构建CA125串联重复序列原核表达载体,确定了最佳可溶性诱导表达条件(0.5 mmol/LIPTG,15℃诱导6 h);Western blot结果证实纯化的重组蛋白正确,纯度高;制备的抗血清能特异识别重组CA125R蛋白和天然CA125糖蛋白。结论:成功建立了CA125R高效原核表达系统,并制备了高纯度重组CA125R蛋白及其抗血清。AIM: To establish a prokaryotic expression system of the tandem repeat of CA125 (CA125R), express and purify the recombinant CA125R protein, prepare its antiserum. METHODS: The full gene sequence of one tandem repeat of CA125 was synthesized and cloned into pET-32a( + ) to construct a prokaryoUc expression vector of the CA125R protein (pET-CA125R). The pET-CA125R was transformed into E. coli BL21 (DE3) and the soluble expres- sion conditions were optimized; the pure recombinant CA125R protein was prepared by affinity Ni-NTA chromatog- raphy and identified by Western blotting. A rabbit was immunized with the pure recombinant CA125R protein to prepare its antiserum. RESULTS: The prokaryotic expres- sion vector of CA125R was successfully constructed. The optimal soluble induction expression conditions were 0.5 mmol/L isopropyl β-D-1-thiogalactopyranoside (IPTG) at 15℃ for 6 h. Western blotting confirmed the pure CAI25R recombi- nant protein of high purity. The prepared antiserum specific- ally recognized recombinant CA125R protein and natural CA125 glycoprotein. CONCLUSION: We successfully es- tablished the efficient prokaryotic expression system of the CA125R, and prepared the recombinant CA125R protein of high purity and its antiserum.
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