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鹅细小病毒NS2基因的克隆和序列分析
引用本文:邢明伟,王君伟,贺云霞,布日额. 鹅细小病毒NS2基因的克隆和序列分析[J]. 中国预防兽医学报, 2003, 25(3): 195-197
作者姓名:邢明伟  王君伟  贺云霞  布日额
作者单位:东北农业大学,动物医学院,黑龙江,哈尔滨,150030
基金项目:黑龙江省“十五”攻关课题 (GB0 1B5 0 2_0 2 )
摘    要:本研究参考CerBank发表的GPV B株全基因序列,设计并合成一对引物,通过PCR技术扩增出GPV H1株NS2基因,目的片段长约1.4kb,将目的片段克隆到pMD18-T载体后进行序列测定和分析,结果表明:GPV H1株NS2基因全长1356bP,编码451个氨基酸,与国外已发表的GPV B株相比核苷酸序列同源性为98.75%,推导氨基酸序列同源性为98.67%。

关 键 词:鹅细小病毒 NS2基因 克隆 序列分析
文章编号:1008-0589(2003)03-0195-03
修稿时间:2002-09-13

Cloning and sequencing of NS2 gene of goose parvovirus
XING Ming_Wei,WANG Jun_wei,HE Yun_xia,Bu Ri_e. Cloning and sequencing of NS2 gene of goose parvovirus[J]. Chinese Journal of Preventive Veterinary Medicine, 2003, 25(3): 195-197
Authors:XING Ming_Wei  WANG Jun_wei  HE Yun_xia  Bu Ri_e
Abstract:According to the sequence of GPV B strain published in GenBank, a pair of primers were designed by Oligo4.0.NS2 gene of GVP and amplified by PCR. The gene of interest was cloned into the vector pMD18_T and sequenced. The results showed that NS2 gene consisted of 1356 nucleotides and encoded 451 amino acids. The NS2 gene shared 98.75 % and 98.67 % homology with that of B isolate at nucleotide and amino acid level, respectively.
Keywords:GPV  NS2 gene  cloning  sequence analysis
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