Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 56
Store in aliquots at – 70°C . Bacteriophage 1 arms Bacteriophage T4 DNA ligase
If you plan to make a large number of libraries , it is much cheaper to prepare
arms by agarose gel electrophoresis ( see Chapter 2 ) than to purchase them .
Store in aliquots at – 70°C . Bacteriophage 1 arms Bacteriophage T4 DNA ligase
If you plan to make a large number of libraries , it is much cheaper to prepare
arms by agarose gel electrophoresis ( see Chapter 2 ) than to purchase them .
Page 54
LABELING THE 3 ' TERMINI OF DOUBLE - STRANDED DNA WITH
BACTERIOPHAGE T4 DNA POLYMERASE Rapid End - labeling of DNA
Bacteriophage T4 DNA polymerase , like the Klenow fragment of E . coli DNA
polymerase I , can be ...
LABELING THE 3 ' TERMINI OF DOUBLE - STRANDED DNA WITH
BACTERIOPHAGE T4 DNA POLYMERASE Rapid End - labeling of DNA
Bacteriophage T4 DNA polymerase , like the Klenow fragment of E . coli DNA
polymerase I , can be ...
Page 31
LABELING OF SYNTHETIC OLIGONUCLEOTIDES BY PHOSPHORYLATION
WITH BACTERIOPHAGE T4 POLYNUCLEOTIDE KINASE Synthetic
oligonucleotides are synthesized without a phosphate group at their 5 ' termini
and are ...
LABELING OF SYNTHETIC OLIGONUCLEOTIDES BY PHOSPHORYLATION
WITH BACTERIOPHAGE T4 POLYNUCLEOTIDE KINASE Synthetic
oligonucleotides are synthesized without a phosphate group at their 5 ' termini
and are ...
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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