Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 9-9
The basic steps used in the construction of libraries of random fragments of
eukaryotic DNA in bacteriophage i vectors are ... separated from the internal
stuffer fragment by any of several methods ( fractionation by size , digestion with
restriction ...
The basic steps used in the construction of libraries of random fragments of
eukaryotic DNA in bacteriophage i vectors are ... separated from the internal
stuffer fragment by any of several methods ( fractionation by size , digestion with
restriction ...
Page 13-38
In addition , because BAL 31 degrades both ends of double - stranded DNA
simultaneously , both the target fragment and ... To obtain viable deletion mutants
, it is therefore almost always necessary to purify the truncated target fragments
by ...
In addition , because BAL 31 degrades both ends of double - stranded DNA
simultaneously , both the target fragment and ... To obtain viable deletion mutants
, it is therefore almost always necessary to purify the truncated target fragments
by ...
Page 15-36
4 - kb BglII DNA fragment containing a kanamycin resistance gene ( kan ' ) .
Because only those linear DNAs containing BglII sites at each end will
incorporate the kan " gene , all bacteria transformed to kanamycin resistance by
the products of ...
4 - kb BglII DNA fragment containing a kanamycin resistance gene ( kan ' ) .
Because only those linear DNAs containing BglII sites at each end will
incorporate the kan " gene , all bacteria transformed to kanamycin resistance by
the products of ...
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LibraryThing Review
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
CONCENTRATING NUCLEIC ACIDS E | 8-10 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
MEASUREMENT OF RADIOACTIVITY IN NUCLEIC ACIDS E | 8-18 |
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Common terms and phrases
aliquots allow amount amplification antibody appropriate approximately bacteriophage bacteriophage T4 base binding buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies complete concentration constructed containing deletions denatured described detection determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filters four fragment gene genomic DNA hybridization increase Incubate inserted interest isolated Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutants nucleic acids nucleotides obtained oligonucleotide plaques plasmid DNA plate position possible precipitation prepared presence primer probe problem protein purified radioactivity radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening separate sequence single single-stranded solution step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume