Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 85
Page 2-83
Digestion of Bacteriophage 1 DNA with Restriction Enzymes 1. Mix 25–50 ug of
bacteriophage 1 DNA with TE ( pH 8.0 ) to give a final volume of 170 ul . 2. Add
20 ul of the appropriate restriction enzyme buffer . Remove two aliquots ( 0.2 ug ...
Digestion of Bacteriophage 1 DNA with Restriction Enzymes 1. Mix 25–50 ug of
bacteriophage 1 DNA with TE ( pH 8.0 ) to give a final volume of 170 ul . 2. Add
20 ul of the appropriate restriction enzyme buffer . Remove two aliquots ( 0.2 ug ...
Page 2-92
Digestion of Bacteriophage à Vectors with Two Restriction Enzymes Vectors such
as the EMBL series , 12001 , ADASH , and Charon 34 , 35 , and 40 contain a
series of restriction sites , arranged in opposite orientations , in polycloning sites
at ...
Digestion of Bacteriophage à Vectors with Two Restriction Enzymes Vectors such
as the EMBL series , 12001 , ADASH , and Charon 34 , 35 , and 40 contain a
series of restriction sites , arranged in opposite orientations , in polycloning sites
at ...
Page 7-64
Incubate for 1-2 hours , depending on the degree of digestion desired . Nuclease
- S1 mapping buffer 0.28 m NaCl 0.05 M sodium acetate ( pH 4.5 ) 4.5 mm
ZnSO4 20 ug / ml single - stranded DNA ( carrier DNA ) 100-1000 units / ml
nuclease ...
Incubate for 1-2 hours , depending on the degree of digestion desired . Nuclease
- S1 mapping buffer 0.28 m NaCl 0.05 M sodium acetate ( pH 4.5 ) 4.5 mm
ZnSO4 20 ug / ml single - stranded DNA ( carrier DNA ) 100-1000 units / ml
nuclease ...
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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
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