Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 49
BLOTTO should not be used in combination with high concentrations of SDS ,
which will cause the ... If background hybridization is a problem , NP - 40 may be
added to the hybridization solution to a final concentration of 1 % . BLOTTO
should ...
BLOTTO should not be used in combination with high concentrations of SDS ,
which will cause the ... If background hybridization is a problem , NP - 40 may be
added to the hybridization solution to a final concentration of 1 % . BLOTTO
should ...
Page 20
Primer : Template Ratios and Nucleotide Concentrations The size , specific
activity , and yield of the radioactive strand ... 1975 ) : effected by the relation
dGTP DCTP DATP DTTP 45 um 200 um 12 um 140 uM When the concentration
of each of ...
Primer : Template Ratios and Nucleotide Concentrations The size , specific
activity , and yield of the radioactive strand ... 1975 ) : effected by the relation
dGTP DCTP DATP DTTP 45 um 200 um 12 um 140 uM When the concentration
of each of ...
Page 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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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 |
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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