Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 75
Page 10-64
Purify the DNA by extraction with phenol : chloroform and precipitation with 2
volumes of ice - cold ethanol for 15 minutes at 0 ° C . Recover the DNA by
centrifugation at 12,000g for 10 minutes at 4 ° C in a microfuge . 2. Dissolve the
DNA in a ...
Purify the DNA by extraction with phenol : chloroform and precipitation with 2
volumes of ice - cold ethanol for 15 minutes at 0 ° C . Recover the DNA by
centrifugation at 12,000g for 10 minutes at 4 ° C in a microfuge . 2. Dissolve the
DNA in a ...
Page 13-96
Incubate 7 minutes at 37 ° C . Incubate 6 minutes at 90 ° C . Incubate 4 minutes at
20 ° C . Chill to 0 ° C . Chill to 0 ° C . Chill to 0 ° C . Add 150 ul 1 M piperidine Add
150 ul 1m piperidine ( at Add 1 ml 1 - butanol . Vortex for ( at 0 ° C ) . 0 ° C ) .
Incubate 7 minutes at 37 ° C . Incubate 6 minutes at 90 ° C . Incubate 4 minutes at
20 ° C . Chill to 0 ° C . Chill to 0 ° C . Chill to 0 ° C . Add 150 ul 1 M piperidine Add
150 ul 1m piperidine ( at Add 1 ml 1 - butanol . Vortex for ( at 0 ° C ) . 0 ° C ) .
Page 15-24
5 minutes , 3 . 0 minutes , 4 . 5 minutes , etc . 3 . Add 36 ul of the appropriate
dilution of BAL 31 ( see step 6 , page 15 . 23 ) to the ... 5 - minute intervals ,
transfer 45 ul of the reaction mixture to the appropriately labeled microfuge tube .
Store the ...
5 minutes , 3 . 0 minutes , 4 . 5 minutes , etc . 3 . Add 36 ul of the appropriate
dilution of BAL 31 ( see step 6 , page 15 . 23 ) to the ... 5 - minute intervals ,
transfer 45 ul of the reaction mixture to the appropriately labeled microfuge tube .
Store 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
Contents
DNA METHYLATION 5 | 8-5 |
SOLUTIONS FOR WORKING WITH BACTERIOPHAGEI A | 8-7 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
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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 isolation 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 vectors volume