Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 73
Ligation to Bacteriophage à Arms Because of the difficulties involved in
determining the molar concentration of the termini of ... The aim is to determine
the amount of cDNA that yields at least 5 x 10° recombinant bacteriophages ( i . e
. , a ...
Ligation to Bacteriophage à Arms Because of the difficulties involved in
determining the molar concentration of the termini of ... The aim is to determine
the amount of cDNA that yields at least 5 x 10° recombinant bacteriophages ( i . e
. , a ...
Page 14
The entire sequence of each strand can then be determined in a single reaction
set using a universal sequencing primer . ... No attempt is made to determine
where these subclones map in the target DNA or which strand of DNA is being ...
The entire sequence of each strand can then be determined in a single reaction
set using a universal sequencing primer . ... No attempt is made to determine
where these subclones map in the target DNA or which strand of DNA is being ...
Page 30
2 unit determined in the exonuclease resistance assay ( Modrich and Lehman
1970 ) and to 60 cohesive - end units ( as defined by New England Biolabs ) . 0 .
015 Weiss unit of bacteriophage T4 DNA ligase therefore will ligate 50 % of the ...
2 unit determined in the exonuclease resistance assay ( Modrich and Lehman
1970 ) and to 60 cohesive - end units ( as defined by New England Biolabs ) . 0 .
015 Weiss unit of bacteriophage T4 DNA ligase therefore will ligate 50 % of the ...
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User Review - iayork - LibraryThingthe BIBLE of every biologist: So few and so much to say about this bible of Biology at the bench... You'll really find everything you want in it, including the composition of all the buffers and ... Read full review
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 |
Copyright | |
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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