Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 8-3
As the enzymatic reactions used to synthesize cDNA have improved , the sizes of
cloned cDNAs have increased , and it is ... In addition , some workers have found
ways to increase the concentration of the relevant mRNA by using drugs to ...
As the enzymatic reactions used to synthesize cDNA have improved , the sizes of
cloned cDNAs have increased , and it is ... In addition , some workers have found
ways to increase the concentration of the relevant mRNA by using drugs to ...
Page 10-36
Contamination of the template with superhelical plasmid DNA will cause an
increase in aberrant initiation of RNA chains ( on both strands of the DNA ) , and
the presence of a protruding 3 ' terminus downstream from the bacteriophage ...
Contamination of the template with superhelical plasmid DNA will cause an
increase in aberrant initiation of RNA chains ( on both strands of the DNA ) , and
the presence of a protruding 3 ' terminus downstream from the bacteriophage ...
Page 13-33
32 ) as a guide , set up a second series of test ligations containing 100 ng of
dephosphorylated vector DNA and increasing concentrations of fragmented ,
bluntended target DNA . 2 . Transform ( phagemid vectors ) or transfect (
bacteriophage ...
32 ) as a guide , set up a second series of test ligations containing 100 ng of
dephosphorylated vector DNA and increasing concentrations of fragmented ,
bluntended target DNA . 2 . Transform ( phagemid vectors ) or transfect (
bacteriophage ...
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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