In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signals

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Veröffentlicht in:Journal of Bacteriology 1980-08, Vol.143 (2), p.971-980
Hauptverfasser: Casadaban, M J, Chou, J, Cohen, S N
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container_title Journal of Bacteriology
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creator Casadaban, M J
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Cohen, S N
description Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue JB About JB Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JB RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0021-9193 Online ISSN: 1098-5530 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to JB .asm.org, visit: JB       
doi_str_mv 10.1128/jb.143.2.971-980.1980
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identifier ISSN: 0021-9193
ispartof Journal of Bacteriology, 1980-08, Vol.143 (2), p.971-980
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1098-5530
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Base Sequence
beta-Galactosidase - genetics
beta-Galactosidase - metabolism
DNA, Recombinant
Escherichia coli - genetics
Galactosidases - genetics
Lac Operon
Plasmids
Protein Biosynthesis
RNA, Bacterial - genetics
RNA, Messenger - genetics
Transcription, Genetic
title In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signals
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