Jiang Zibin, Li Yuan
Institute of Medicinal Biotechnology, Peking Union Medical College, Chinese Academy of Medical Science, Beijing 100050, China.
Wei Sheng Wu Xue Bao. 2002 Aug;42(4):411-7.
Using RNA extracted from human umbilical vein endothelium cell as a template, the gene VEGF receptor Flt-1 was amplified by RT-PCR. Recombinant plasmid pSGLgpp-F was constructed and was transformed into S. lividans TK24. With the detection of SDS-PAGE and Western blot, a specific band being same to the reports near 63.6 kd was found. The results showed sFlt-1 was successfully expressed in S. lividans. The result of the binding assay of receptor-ligand for sFlt-1 showed sFlt-1 has the biological activity of binding with its ligand VEGF.
以人脐静脉内皮细胞提取的RNA为模板,通过RT-PCR扩增VEGF受体Flt-1基因。构建重组质粒pSGLgpp-F并将其转化到变铅青链霉菌TK24中。通过SDS-PAGE和Western blot检测,在63.6 kd附近发现一条与报道一致的特异性条带。结果表明sFlt-1在变铅青链霉菌中成功表达。sFlt-1受体-配体结合试验结果表明sFlt-1具有与其配体VEGF结合的生物活性。