Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 11
EXPRESSION OF PROKARYOTIC GENES : PROMOTERS The first step in
expressing eukaryotic proteins in bacteria is to choose an expression vector that
carries a strong , regulated prokaryotic promoter . Here we describe the use of ...
EXPRESSION OF PROKARYOTIC GENES : PROMOTERS The first step in
expressing eukaryotic proteins in bacteria is to choose an expression vector that
carries a strong , regulated prokaryotic promoter . Here we describe the use of ...
Page 13
The trp - lac Promoter Another promoter that has been used successfully to
produce large amounts of proteins in E . coli is the tac promoter , a hybrid trp - lac
promoter that is regulated by lac repressor ( Amann et al . 1983 ; de Boer et al .
The trp - lac Promoter Another promoter that has been used successfully to
produce large amounts of proteins in E . coli is the tac promoter , a hybrid trp - lac
promoter that is regulated by lac repressor ( Amann et al . 1983 ; de Boer et al .
Page 15
The Bacteriophage T7 Promoter A novel expression system has been developed
by Studier and Moffatt ( 1986 ) and Tabor and Richardson ( 1985 ) using a
bacteriophage T7 RNA polymerase / promoter system . This system is designed
for ...
The Bacteriophage T7 Promoter A novel expression system has been developed
by Studier and Moffatt ( 1986 ) and Tabor and Richardson ( 1985 ) using a
bacteriophage T7 RNA polymerase / promoter system . This system is designed
for ...
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Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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acetate activity added Adjust aliquots allow amount antibody antigen Appendix appropriate approximately aqueous assay bacterial bacteriophage base binding buffer carried cells centrifugation Chapter chromatography Cl pH cloned coli column complete concentration containing culture deionized water described desired detected dilution Dissolve EDTA efficiency electrophoresis enzyme et al ethanol expression extract Figure filter final fragment gene growth hybridization Incubate levels ligation mammalian cells medium method mg/ml microfuge tube minutes mixture mRNAs nucleic acid pellet phase phosphate Place plasmid plate polymerase precipitation prepared procedure Products promoter protein radioactive radiolabeled reaction remove restriction room temperature sample screen selection sequence sodium solution specific step sterile stored strain TABLE Telephone termini tion transcription transfection transfer transformation Tris ug/ml usually vectors volume wash western blotting ОН