Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 148
Remove the supernatant as completely as possible , and store the open tube for
a few minutes in an inverted position on a pad of paper towels at room
temperature to allow the last traces of ethanol to drain away . 7. Wash the pellet
with 70 ...
Remove the supernatant as completely as possible , and store the open tube for
a few minutes in an inverted position on a pad of paper towels at room
temperature to allow the last traces of ethanol to drain away . 7. Wash the pellet
with 70 ...
Page 6-44
Use just enough staining solution to cover the gel completely . After staining for
30-45 minutes at room temperature , remove the gel , using the glass plate as a
support . Carefully blot excess liquid from the surface of the gel with a pad of ...
Use just enough staining solution to cover the gel completely . After staining for
30-45 minutes at room temperature , remove the gel , using the glass plate as a
support . Carefully blot excess liquid from the surface of the gel with a pad of ...
Page 7-33
Transfer each gel slice to a polypropylene tube , and add at least 4 volumes of
0.5 m ammonium acetate preheated to 65 ° C . Be sure to use a large volume of
ammonium acetate so that the gel slice dissolves completely . Otherwise ,
agarose ...
Transfer each gel slice to a polypropylene tube , and add at least 4 volumes of
0.5 m ammonium acetate preheated to 65 ° C . Be sure to use a large volume of
ammonium acetate so that the gel slice dissolves completely . Otherwise ,
agarose ...
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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
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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