Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 81
Page 123
With the one exception referred to in number 3 above , any method can therefore
be used with any strain of E. coli grown in cultures of any size . It is curious ,
however , that many laboratories use one method to rocess minipreps and
another ...
With the one exception referred to in number 3 above , any method can therefore
be used with any strain of E. coli grown in cultures of any size . It is curious ,
however , that many laboratories use one method to rocess minipreps and
another ...
Page 1-12
See Dideoxy- mediated chain-termination (Sanger) method for DNA sequence
analysis; DNA sequence analysis; Maxam and Gilbert chemical degradation of
DNA method for DNA sequence analysis; Nucleotide sequence data banks ...
See Dideoxy- mediated chain-termination (Sanger) method for DNA sequence
analysis; DNA sequence analysis; Maxam and Gilbert chemical degradation of
DNA method for DNA sequence analysis; Nucleotide sequence data banks ...
Page 1-5
Calcium phosphate - DNA transfection of mammalian cells ( continued ) adherent
cells in suspension , method , 16.37 cells growing in suspension , method , 16.38
modified ( Chen and Okayama ) method , 16.39-16.40 Calf intestinal alkaline ...
Calcium phosphate - DNA transfection of mammalian cells ( continued ) adherent
cells in suspension , method , 16.37 cells growing in suspension , method , 16.38
modified ( Chen and Okayama ) method , 16.39-16.40 Calf intestinal alkaline ...
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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