Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 83
Page 129
Remove the pellet of bacterial debris from the microfuge tube with a sterile
toothpick . 6. Add to the supernatant 40 ul of ... 7. Recover the pellet of nucleic
acids by centrifugation at 12,000g for 5 minutes at 4 ° C in a microfuge . 8.
Remove the ...
Remove the pellet of bacterial debris from the microfuge tube with a sterile
toothpick . 6. Add to the supernatant 40 ul of ... 7. Recover the pellet of nucleic
acids by centrifugation at 12,000g for 5 minutes at 4 ° C in a microfuge . 8.
Remove the ...
Page 2-83
Add 20 ul of the appropriate restriction enzyme buffer . Remove two aliquots ( 0.2
ug each ) of the undigested DNA and store on ice . 3. Add a threefold excess ( 75
-150 units ) of the appropriate restriction enzyme and incubate for 1 hour at the ...
Add 20 ul of the appropriate restriction enzyme buffer . Remove two aliquots ( 0.2
ug each ) of the undigested DNA and store on ice . 3. Add a threefold excess ( 75
-150 units ) of the appropriate restriction enzyme and incubate for 1 hour at the ...
Page 7-16
Precipitation of the RNA with lithium chloride is helpful in removing glycoproteins
and yolky components from the preparations . No attempt is made to remove
DNA from the preparation , since the amount of RNA obtained greatly exceeds
the ...
Precipitation of the RNA with lithium chloride is helpful in removing glycoproteins
and yolky components from the preparations . No attempt is made to remove
DNA from the preparation , since the amount of RNA obtained greatly exceeds
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
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
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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