Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 56
Fix the proteins by incubating the gel for 4 - 12 hours at room temperature with
gentle shaking in at least 5 gel volumes of a solution of ethanol : glacial acetic
acid : water ( 30 : 10 : 60 ) . 2 . Discard the fixing solution , and add at least 5 gel ...
Fix the proteins by incubating the gel for 4 - 12 hours at room temperature with
gentle shaking in at least 5 gel volumes of a solution of ethanol : glacial acetic
acid : water ( 30 : 10 : 60 ) . 2 . Discard the fixing solution , and add at least 5 gel ...
Page 10
CONCENTRATING NUCLEIC ACIDS Precipitation with Ethanol or Isopropanol
The most widely used method for concentrating nucleic acids is precipitation with
ethanol . The precipitate of nucleic acid , which is allowed to form in the presence
...
CONCENTRATING NUCLEIC ACIDS Precipitation with Ethanol or Isopropanol
The most widely used method for concentrating nucleic acids is precipitation with
ethanol . The precipitate of nucleic acid , which is allowed to form in the presence
...
Page 14
less volatile than ethanol and is therefore more difficult to remove ; moreover ,
solutes such as sucrose or sodium chloride are more easily coprecipitated with
DNA when isopropanol is used . In general , precipitation with ethanol is
preferable ...
less volatile than ethanol and is therefore more difficult to remove ; moreover ,
solutes such as sucrose or sodium chloride are more easily coprecipitated with
DNA when isopropanol is used . In general , precipitation with ethanol is
preferable ...
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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