Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 25
Following construction and amplification in bacteria , recombinant BPV DNAs are
transfected into cultured mammalian cells , usually by the calcium phosphate
coprecipitation technique ( see pages 16 . 32 – 16 . 40 ) . If a selectable marker is
...
Following construction and amplification in bacteria , recombinant BPV DNAs are
transfected into cultured mammalian cells , usually by the calcium phosphate
coprecipitation technique ( see pages 16 . 32 – 16 . 40 ) . If a selectable marker is
...
Page 37
Protoplasts formed by the action of zymolase will be visible in the untreated
sample but should be lysed in the sample containing detergent . Continue
incubation until the majority of the cells have been converted to protoplasts . This
usually ...
Protoplasts formed by the action of zymolase will be visible in the untreated
sample but should be lysed in the sample containing detergent . Continue
incubation until the majority of the cells have been converted to protoplasts . This
usually ...
Page 79
Then , using the optimum concentration of magnesium acetate , determine the
effect of different concentrations of KCI ( 20 – 80 mm ) on the efficiency of
translation of the particular mRNA of interest . Approximately 70 mM KCl is
usually optimal ...
Then , using the optimum concentration of magnesium acetate , determine the
effect of different concentrations of KCI ( 20 – 80 mm ) on the efficiency of
translation of the particular mRNA of interest . Approximately 70 mM KCl is
usually optimal ...
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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