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LAMBDA-GT22S, A PHAGE EXPRESSION VECTOR FOR THE DIRECTIONAL CLONING OF CDNA BY THE USE OF A SINGLE RESTRICTION ENZYME SFII

被引：8
作者：
HAN, JH
RUTTER, WJ
机构：
[1] UNIV CALIF SAN FRANCISCO,HORMONE RES INST,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94143
来源：
NUCLEIC ACIDS RESEARCH | 1988年 / 16卷 / 24期
关键词：
D O I：
10.1093/nar/16.24.11837
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：11837 / 11837
页数：1
相关论文
共 6 条
[1]   ENZYMATIC AMPLIFICATION OF SPECIFIC CDNA INSERTS FROM LAMBDA-GT11 LIBRARIES [J].
FRIEDMAN, KD ;
ROSEN, NL ;
NEWMAN, PJ ;
MONTGOMERY, RR .
NUCLEIC ACIDS RESEARCH, 1988, 16 (17) :8718-8718
[2]  
Han J., UNPUB
[3]   ISOLATION OF FULL-LENGTH PUTATIVE RAT LYSOPHOSPHOLIPASE CDNA USING IMPROVED METHODS FOR MESSENGER-RNA ISOLATION AND CDNA CLONING [J].
HAN, JH ;
STRATOWA, C ;
RUTTER, WJ .
BIOCHEMISTRY, 1987, 26 (06) :1617-1625
[4]   LAMBDA-GT22, AN IMPROVED LAMBDA-VECTOR FOR THE DIRECTIONAL CLONING OF FULL-LENGTH CDNA [J].
HAN, JH ;
RUTTER, WJ .
NUCLEIC ACIDS RESEARCH, 1987, 15 (15) :6304-6304
[5]  
HAN JH, 1988, GENETIC ENG, V10, P195
[6]  
HAN JH, 1989, IN PRESS GENE
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