Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 83
Page xxiv
Analysis of Genomic DNA by Southern Hybridization 9.31 SEPARATION OF
RESTRICTION FRAGMENTS OF MAMMALIAN GENOMIC DNA BY AGAROSE
GEL ELECTROPHORESIS 9.32 TRANSFER OF DNA FROM AGAROSE GELS
TO ...
Analysis of Genomic DNA by Southern Hybridization 9.31 SEPARATION OF
RESTRICTION FRAGMENTS OF MAMMALIAN GENOMIC DNA BY AGAROSE
GEL ELECTROPHORESIS 9.32 TRANSFER OF DNA FROM AGAROSE GELS
TO ...
Page 2-110
Once in contact with the top agarose , the filter wets very rapidly and transfer of
bacteriophage DNA occurs quickly . Therefore , do not move the filter once
contact with the plate is made . The easiest way to place the filter on the plate is
to hold ...
Once in contact with the top agarose , the filter wets very rapidly and transfer of
bacteriophage DNA occurs quickly . Therefore , do not move the filter once
contact with the plate is made . The easiest way to place the filter on the plate is
to hold ...
Page 7-51
Staining RNA Before and After Transfer to Nitrocellulose Filters Prolonged
staining with ethidium bromide is not recommended before RNA is transferred
from agarose gels to nitrocellulose filters because saturation of the nucleic acid
with the ...
Staining RNA Before and After Transfer to Nitrocellulose Filters Prolonged
staining with ethidium bromide is not recommended before RNA is transferred
from agarose gels to nitrocellulose filters because saturation of the nucleic acid
with the ...
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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