Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 62
Extract the mixture once with chloroform , and precipitate the DNA with 2 volumes
of ice - cold ethanol . Store the tube on ice for 15 minutes , and then collect the
precipitated DNA by centrifugation at 12 , 000g for 10 minutes at 4°C in a ...
Extract the mixture once with chloroform , and precipitate the DNA with 2 volumes
of ice - cold ethanol . Store the tube on ice for 15 minutes , and then collect the
precipitated DNA by centrifugation at 12 , 000g for 10 minutes at 4°C in a ...
Page 65
Collect the precipitate by centrifugation at 12 , 000g for 20 minutes at 4°C in a
microfuge . Wash the pellet with ice - cold 70 % ethanol and recentrifuge . Allow
the precipitate to dry completely at room temperature before dissolving it in TE (
pH ...
Collect the precipitate by centrifugation at 12 , 000g for 20 minutes at 4°C in a
microfuge . Wash the pellet with ice - cold 70 % ethanol and recentrifuge . Allow
the precipitate to dry completely at room temperature before dissolving it in TE (
pH ...
Page 35
Purification of Radiolabeled Oligonucleotides by Precipitation with
Cetylpyridinium Bromide This method , which was ... The detergent is then
removed from the precipitate with ethanol ( in which the nucleic acids are
insoluble ) , and the ...
Purification of Radiolabeled Oligonucleotides by Precipitation with
Cetylpyridinium Bromide This method , which was ... The detergent is then
removed from the precipitate with ethanol ( in which the nucleic acids are
insoluble ) , and 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