Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 85
Page 9-49
BLOTTO should not be used in combination with high concentrations of SDS ,
which will ... If background hybridization is a problem , NP - 40 may be added to
the hybridization solution to a final concentration of 1 % . BLOTTO should not be
...
BLOTTO should not be used in combination with high concentrations of SDS ,
which will ... If background hybridization is a problem , NP - 40 may be added to
the hybridization solution to a final concentration of 1 % . BLOTTO should not be
...
Page 10-20
Primer : Template Ratios and Nucleotide Concentrations The size , specific
activity , and yield of the radioactive strand ... 1975 ) : dGTP MCTP DATP dTTP 45
um 200 um 12 um 140 uM When the concentration of each of the four dNTPs in
the ...
Primer : Template Ratios and Nucleotide Concentrations The size , specific
activity , and yield of the radioactive strand ... 1975 ) : dGTP MCTP DATP dTTP 45
um 200 um 12 um 140 uM When the concentration of each of the four dNTPs in
the ...
Page 10-32
More than 90 % of the transcripts are full - length when the concentration of each
of the rNTPs is 50 um or greater . Because bacteriophage SP6 DNA - dependent
RNA polymerase is more tolerant of lower concentrations of rGTP than of the ...
More than 90 % of the transcripts are full - length when the concentration of each
of the rNTPs is 50 um or greater . Because bacteriophage SP6 DNA - dependent
RNA polymerase is more tolerant of lower concentrations of rGTP than of the ...
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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
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Common terms and phrases
activity addition aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleavage cleaved clones complete concentration constructed containing deletions denatured described determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filter four fragment gene genomic DNA hybridization increase Incubate inserted interest isolation Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutations nucleic acids nucleotides obtained oligonucleotide original 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 specific step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume