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Chinese Journal of Hematology ; (12): 5-8, 2002.
Artigo em Chinês | WPRIM | ID: wpr-314654

RESUMO

<p><b>OBJECTIVE</b>To construct a vector containing protein transduction domain (PTD) and bcr/abl fusion gene of chronic myelogenous leukemia and express PTD-bcr/abl fusion protein in E. Coli.</p><p><b>METHODS</b>DNA fragment encoding PTD was synthesized and fused to PCR-amplified bcr/abl gene fragment, then inserted into plasmid pET-16b to get the expression vector pEPb containing PTD-bcr/abl fusion gene, which was transfected and expressed in E. Coli LB21. PTD-bcr/abl fusion protein was purified by affinity chromatography.</p><p><b>RESULTS</b>523 bp bcr/abl fusion gene was effectively amplified. The PTD-bcr/abl gene sequencing showed the same sequence as scheduled. The fusion peptide was successfully expressed in E. Coli and purified.</p><p><b>CONCLUSION</b>The results may provide a new PTD-bcr/abl fusion peptide for the immunotherapy of CML.</p>


Assuntos
Eletroforese em Gel de Poliacrilamida , Escherichia coli , Genética , Proteínas de Fusão bcr-abl , Genética , Metabolismo , Expressão Gênica , Produtos do Gene tat , Genética , Metabolismo , Vetores Genéticos , Genética , Leucemia Mielogênica Crônica BCR-ABL Positiva , Genética , Proteínas Recombinantes de Fusão , Genética , Metabolismo
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