DIRECT CLONING OF POLYMERASE CHAIN-REACTION PRODUCTS IN AN XCMI T-VECTOR

被引：31

作者：

HARRISON, J

MOLLOY, PL

CLARK, SJ

机构：

[1] CSIRO,DIV BIOMOLEC ENGN,SYDNEY LAB,N RYDE,NSW 2113,AUSTRALIA

[2] ROYAL PRINCE ALFRED HOSP,KANEMATSU LABS,CAMPERDOWN,NSW 2050,AUSTRALIA

来源：

ANALYTICAL BIOCHEMISTRY | 1994年 / 216卷 / 01期

关键词：

D O I：

10.1006/abio.1994.1033

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

收藏

页码：235 / 236

页数：2

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[J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (20) : 9677 - 9686
[2] A SIMPLE METHOD FOR SITE-DIRECTED MUTAGENESIS USING THE POLYMERASE CHAIN-REACTION
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[J]. GENE, 1993, 130 (01) : 153 - 154
[4] GENERAL-METHOD FOR DIRECT CLONING OF DNA FRAGMENTS GENERATED BY THE POLYMERASE CHAIN-REACTION
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[J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (16) : 4560 - 4560
[5] CONSTRUCTION OF T-VECTORS, A RAPID AND GENERAL SYSTEM FOR DIRECT CLONING OF UNMODIFIED PCR PRODUCTS
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[J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (05) : 1154 - 1154