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加工番茄多聚半乳糖醛酸酶(PG)基因的cDNA克隆
引用本文:李惠,肖璐,祝建波,崔百明,乐锦华,曹连莆.加工番茄多聚半乳糖醛酸酶(PG)基因的cDNA克隆[J].石河子大学学报,2000,4(3):220-222,252.
作者姓名:李惠  肖璐  祝建波  崔百明  乐锦华  曹连莆
作者单位:[1]石河子大学农学院农业科学系 [2]石河子大学生物科学系
摘    要:以加工番茄87-5为材料,运用反转录PCR(RT-PCR)技术成功地将PG基因的cDNA序列克隆到pGEM-T载体上,并利用酶切及PCR进行了初步鉴定。

关 键 词:RT-PCR  cDNA  PG基因  克隆  番茄  转基因育种
文章编号:1007-7383(2000)03-0220-13

Clonging the cDNA of Polygaacturonase in Processing Tomato
LI Hui\ ,\ XIAO Lu\ ,\ ZHU Jian bo\ ,\ CUI Bai ming\ ,\ LE Jin hua\ ,\ CAO Lian pu\.Clonging the cDNA of Polygaacturonase in Processing Tomato[J].Journal of Shihezi University(Natural Science),2000,4(3):220-222,252.
Authors:LI Hui\  \ XIAO Lu\  \ ZHU Jian bo\  \ CUI Bai ming\  \ LE Jin hua\  \ CAO Lian pu\
Institution:LI Hui\ 1,\ XIAO Lu\ 2,\ ZHU Jian bo\ 2,\ CUI Bai ming\ 2,\ LE Jin hua\ 2,\ CAO Lian pu\ 1
Abstract:The entire cDNA encoding polygalacturonase was successfully cloned with RT PCR technique from pericarp of ripe processing tomato fruits 87 5,and its whole nucleotide sequence was tentatively analysed and identified.
Keywords:cDNA encoding polygalacturonase  RT  PCR  PG cDNA  clone
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