Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 12-4
More commonly, however, the foreign DNA sequences are cloned into a
restriction site that lies within the coding sequences of a prokaryotic gene (or
fragment of a gene) located immediately downstream from the promoter /
ribosome-binding ...
More commonly, however, the foreign DNA sequences are cloned into a
restriction site that lies within the coding sequences of a prokaryotic gene (or
fragment of a gene) located immediately downstream from the promoter /
ribosome-binding ...
Page 1-2
See BAP; CIP a-Complementation of defective 0- galactosidase histochemical
identification of recombinant clones, 1.85-1.86, 4.7-4.8 and lacZ AM 15 on F' in
bacteriophage M13 host strains, 4.12 and plaque screening of bacteriophage
M13, ...
See BAP; CIP a-Complementation of defective 0- galactosidase histochemical
identification of recombinant clones, 1.85-1.86, 4.7-4.8 and lacZ AM 15 on F' in
bacteriophage M13 host strains, 4.12 and plaque screening of bacteriophage
M13, ...
Page 1-4
... generation of nested sets of deletion mutants for DNA sequence analysis,
13.34-13.35 BAP (bacterial alkaline phosphatase) activity and uses, 5.72
inactivation after reaction, 5.72 suppression of self-ligation of plasmid cloning
vectors, 1.56.
... generation of nested sets of deletion mutants for DNA sequence analysis,
13.34-13.35 BAP (bacterial alkaline phosphatase) activity and uses, 5.72
inactivation after reaction, 5.72 suppression of self-ligation of plasmid cloning
vectors, 1.56.
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Contents
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
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Common terms and phrases
acid activity agarose aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies concentration constructed containing deletions denatured described determine digestion DNA polymerase dNTPs double-stranded efficiency electrophoresis et al ethanol expression Figure filters fragment gene genomic hybridization increase Incubate inserted interest isolated labeled length libraries ligation linear linkers method microfuge minutes mixture molecules mRNA mutagenesis mutagenic mutations Nucleic nucleotides obtained oligonucleotide original plaques plasmid plasmid DNA plate pool position possible prepared presence primer probe problem protein purified radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening sequence single single-stranded solution specific step Store strand synthesis target DNA target sequence template termini tion transfer transformants tube units usually vector volume