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作 者:王元利[1,2] 张宏斌[1,2] 王捷[1,2] 杨太成 江悦华[1,2] 于茂生
机构地区:[1]广州军区广州总医院泌尿外科 [2]第四军医大学西京医院泌尿外科
出 处:《中华泌尿外科杂志》1998年第3期131-134,共4页Chinese Journal of Urology
基 金:国家自然科学基金
摘 要:应用PCR方法,从分泌鼠抗人膀胱癌抗体的杂交瘤细胞中扩增抗体重、轻链可变区基因,经DNA接头连接后与噬菌粒pCANTAB5重组,转化大肠杆菌后,通过亲和筛选、再转染、克隆及鉴定,以此获得抗人膀胱癌噬菌体单链抗体。Using polymerase chain reaction, the immunoglobulin variable region genes were amplified from antihuman bladder cancer hybridomas cells. The heavy and light chain DNA products were assembled into a single gene using a DNA linker. The antibladder cancer single chain DNA fragment was ligated into a phagemid vector pCANTAB5, and the recombinant vector was subsequently introduced into E. coli TG1 cells for construction of phage display libraries of antihuman bladder cancer. By affinity selection, the antihuman bladder cancer single chain antibody of defined specificity and affinity was obtained.
分 类 号:R392-33[医药卫生—免疫学] R737.140.5[医药卫生—基础医学]
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