Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 139
The precipitate that forms during storage at 0 ° C consists of chromosomal DNA ,
high - molecular - weight RNA , and potassium / SDS / protein / membrane
complexes . 5. Centrifuge the bacterial lysate at 4000 rpm for 15 minutes at 4 ° C
in a ...
The precipitate that forms during storage at 0 ° C consists of chromosomal DNA ,
high - molecular - weight RNA , and potassium / SDS / protein / membrane
complexes . 5. Centrifuge the bacterial lysate at 4000 rpm for 15 minutes at 4 ° C
in a ...
Page 2-73
Cool in ice water and let stand for at least 1 hour on ice to allow the
bacteriophage particles to form a precipitate . 6. Recover the precipitated
bacteriophage particles by centrifugation at 11,000g for 10 minutes at 4 ° C .
Discard the supernatant ...
Cool in ice water and let stand for at least 1 hour on ice to allow the
bacteriophage particles to form a precipitate . 6. Recover the precipitated
bacteriophage particles by centrifugation at 11,000g for 10 minutes at 4 ° C .
Discard the supernatant ...
Page 4-32
Stirring for longer periods of time can result in the precipitation of undesired
bacterial debris . 3. Collect the precipitate by centrifugation at 10,000g for 20
minutes at 4 ° C . Let the centrifuge bottle stand in an inverted position for 2-3
minutes to ...
Stirring for longer periods of time can result in the precipitation of undesired
bacterial debris . 3. Collect the precipitate by centrifugation at 10,000g for 20
minutes at 4 ° C . Let the centrifuge bottle stand in an inverted position for 2-3
minutes to ...
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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 agar agarose aliquots allow amount appropriate arms bacterial bacteriophage BamHI buffer carrying cells centrifugation Chapter cloning coli colonies completely concentration construction containing cosmid culture described digestion EcoRI efficiency electrophoresis et al ethanol ethidium ethidium bromide extracts Figure filters final foreign DNA fragments gene genetic genome growth Hindi host hybridization Incubate infected inserted libraries ligase ligation linear method microfuge minutes minutes at 4°C mixture molecules mutations nucleic acids obtained original packaging particles pellet plaques plasmid DNA plate polycloning polymerase possible precipitate prepared presence probes problem procedure promoter protein purified reaction recombinant Recover region remove replication restriction enzyme room temperature Sall segment selection sequences single single-stranded Smal solution step sterile stored strains strand supernatant termini transfer transformation tube usually vector volume Xbal yield