Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 71
Page 6-26
Carefully rinse the pellet with 70 % ethanol , and then redissolve the DNA in 3-5
ul of TE ( pH 7.6 ) . The addition of 10 ug of carrier RNA before precipitation may
improve the recovery of small amounts of DNA . However , before adding the ...
Carefully rinse the pellet with 70 % ethanol , and then redissolve the DNA in 3-5
ul of TE ( pH 7.6 ) . The addition of 10 ug of carrier RNA before precipitation may
improve the recovery of small amounts of DNA . However , before adding the ...
Page 7-21
Fill the bottom of the tube with 70 % ethanol at room temperature . Invert the tube
and drain off the ethanol , again checking that the pellet of RNA is not dislodged .
Washing with ethanol removes CsCl from the pellet of RNA , making it easier to ...
Fill the bottom of the tube with 70 % ethanol at room temperature . Invert the tube
and drain off the ethanol , again checking that the pellet of RNA is not dislodged .
Washing with ethanol removes CsCl from the pellet of RNA , making it easier to ...
Page 7-82
Stock solutions of actinomycin D are usually prepared in ethanol at a
concentration of 5 mg / ml , stored at -20 ° C in the dark , and diluted into the
reaction mixture immediately before use . Caution : Actinomycin D is a teratogen
and a ...
Stock solutions of actinomycin D are usually prepared in ethanol at a
concentration of 5 mg / ml , stored at -20 ° C in the dark , and diluted into the
reaction mixture immediately before use . Caution : Actinomycin D is a teratogen
and a ...
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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