Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
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Page 180
Immediately snap - freeze the competent cells by immersing the tightly closed
tubes in liquid nitrogen . Store the tubes at – 70 ° C until needed . For most
cloning purposes , 50 - ul aliquots of the competent - cell suspension will be more
than ...
Immediately snap - freeze the competent cells by immersing the tightly closed
tubes in liquid nitrogen . Store the tubes at – 70 ° C until needed . For most
cloning purposes , 50 - ul aliquots of the competent - cell suspension will be more
than ...
Page 6-53
Intact cells or nuclei are resuspended in molten , low - meltingtemperature
agarose and solidified in blocks whose size ... Depending on the organism , any
of a variety of substances are infused into the plug to cause lysis of the cells and
...
Intact cells or nuclei are resuspended in molten , low - meltingtemperature
agarose and solidified in blocks whose size ... Depending on the organism , any
of a variety of substances are infused into the plug to cause lysis of the cells and
...
Page 7-12
Isolation of Cytoplasmic RNA from Mammalian Cells This is a convenient and
well - tested procedure for purifying ... RNA prepared in this way is an excellent
template for the preparation of cDNA libraries , for cell - free translation , and for ...
Isolation of Cytoplasmic RNA from Mammalian Cells This is a convenient and
well - tested procedure for purifying ... RNA prepared in this way is an excellent
template for the preparation of cDNA libraries , for cell - free translation , and for ...
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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