Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 63
The acetylated chloramphenicol partitions into the organic phase , and the acetyl
coenzyme A remains in the aqueous phase . Extracts of transfected cells ,
prepared as described on pages 16 . 59 and 16 . 60 , steps 1 - 3 ( except reserve
30 ul ...
The acetylated chloramphenicol partitions into the organic phase , and the acetyl
coenzyme A remains in the aqueous phase . Extracts of transfected cells ,
prepared as described on pages 16 . 59 and 16 . 60 , steps 1 - 3 ( except reserve
30 ul ...
Page 3
The nucleic acid will tend to partition into the organic phase if the phenol has not
been adequately equilibrated to a pH of 7 . ... If the organic and aqueous phases
are not well - separated , centrifuge again for a longer time or at a higher speed .
The nucleic acid will tend to partition into the organic phase if the phenol has not
been adequately equilibrated to a pH of 7 . ... If the organic and aqueous phases
are not well - separated , centrifuge again for a longer time or at a higher speed .
Page 16
If this happens , add water to the organic phase until an aqueous phase ( which
should contain the nucleic acid ) reappears . 2 . Centrifuge the solution at room
temperature at 12 , 000g for 20 seconds in a microfuge or at 1600g for 1 minute
in ...
If this happens , add water to the organic phase until an aqueous phase ( which
should contain the nucleic acid ) reappears . 2 . Centrifuge the solution at room
temperature at 12 , 000g for 20 seconds in a microfuge or at 1600g for 1 minute
in ...
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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
Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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Common terms and phrases
acetate activity added Adjust aliquots allow amount antibody antigen Appendix appropriate approximately aqueous assay bacterial bacteriophage base binding buffer carried cells centrifugation Chapter chromatography Cl pH cloned coli column complete concentration containing culture deionized water described desired detected dilution Dissolve EDTA efficiency electrophoresis enzyme et al ethanol expression extract Figure filter final fragment gene growth hybridization Incubate levels ligation mammalian cells medium method mg/ml microfuge tube minutes mixture mRNAs nucleic acid pellet phase phosphate Place plasmid plate polymerase precipitation prepared procedure Products promoter protein radioactive radiolabeled reaction remove restriction room temperature sample screen selection sequence sodium solution specific step sterile stored strain TABLE Telephone termini tion transcription transfection transfer transformation Tris ug/ml usually vectors volume wash western blotting ОН