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人白细胞介素-10 cDNA的克隆、测序和真核表达载体的构建
引用本文:代文杰,姜洪池,潘尚哈,吕晓颖.人白细胞介素-10 cDNA的克隆、测序和真核表达载体的构建[J].哈尔滨医科大学学报,2001,35(1):4-6.
作者姓名:代文杰  姜洪池  潘尚哈  吕晓颖
作者单位:1. 哈尔滨医科大学附属第一医院 普外二科
2. 实验诊断室,黑龙江 哈尔滨 150001
基金项目:National natural science foundation(30070739)
摘    要:目的 克隆、测序人白细胞介素-10 cDNA开放阅读框架。方法 刀豆蛋白A活化的人外周血核细胞培养后用于提取总RNA,以随机引物行逆转录反应合成hIL-10 cDNA第一链,并以hIL-10 特异性引物行PCR扩增,将PCR产物克隆至pUC18中测序并构建真核表达载体pcDNA3.1hIL-10。结果 PCR扩出550bp特异性片段,经克隆至pUC18后测序表明序列同源性与GenBank报道完全一致,并克隆鉴定了真核表达载体pcDNA3.1hIL-10。结论 成功克隆了人白细胞介素-10 cDNA开放阅读框架,序列分析证实与GenBank录入序列同源性达100%,并成功构建了真核表达载体pcDNA3.1hIL-10。

关 键 词:克隆  序列分析  人白细胞介素-10  真核表达载体  CDNA
文章编号:1000-1905(2001)01-0004-03
修稿时间:2000年7月6日

Cloning,sequencing of human interleukin 10 cDNA and construction of its eukaryotic expression vector
DAI Wen-jie.Cloning,sequencing of human interleukin 10 cDNA and construction of its eukaryotic expression vector[J].Journal of Harbin Medical University,2001,35(1):4-6.
Authors:DAI Wen-jie
Abstract:Objective To clone open reading frame(ORF) of human interleukin 10 (hIL 10) cDNA for subsequent construction of eukaryotic expression vector.Methods Concanavalin A activated mononuclear cells from peripheral blood were cultured for total RNA extraction.With the use of random primers,cDNA was synthesized and then PCR was accomplished using the specific human interleukin 10 primers.Sequence analysis of pUC18hIL 10 was achieved with 377 type DNA sequencer;Eukaryotic expression vector pcDNA3.1hIL 10 was constructed with ligation.Results A 550bp DNA fragment was amplified with RT PCR.pUC18hIL 10 and pcDNA3.1hIL 10 were constructed and sequence analysis revealed 100% homology to published data in GenBank.Conclusion We successfully cloned human interleukin 10 cDNA ORF and constructed the eukaryotic expression vector pcDNA3.1hIL 10.
Keywords:clone  sequence analysis  interleukin 10  human  expression vector  eukaryotic
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