Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 79
Page 8-75
Incubate the plates for 8 – 10 hours at 42°C . Plaque formation with AZAP : Grow
E . coli strain BB4 in NZCYM medium containing 0 . 2 % maltose . Prepare a
stock of plating bacteria in 10 mM MgSO , as described in Chapter 2 , page 2 . 60
.
Incubate the plates for 8 – 10 hours at 42°C . Plaque formation with AZAP : Grow
E . coli strain BB4 in NZCYM medium containing 0 . 2 % maltose . Prepare a
stock of plating bacteria in 10 mM MgSO , as described in Chapter 2 , page 2 . 60
.
Page 12-23
Incubate the plate for 2-4 hours at 37 ° C . To induce synthesis in expression
vectors that carry the bacteriophage 1 PR promoter ( e.g. , the pEX vectors ; see
Chapter 17 ) , transfer the filter to a prewarmed plate and incubate for 2-4 hours
at 42 ...
Incubate the plate for 2-4 hours at 37 ° C . To induce synthesis in expression
vectors that carry the bacteriophage 1 PR promoter ( e.g. , the pEX vectors ; see
Chapter 17 ) , transfer the filter to a prewarmed plate and incubate for 2-4 hours
at 42 ...
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 ) .
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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
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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