Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 32
PMSF , which is labile in aqueous solution , should be added from a stock
solution just before the lysis buffer is used . The rate of inactivation in aqueous
solution increases with pH and is faster at 25°C than at 4°C . The half - life of a 20
um ...
PMSF , which is labile in aqueous solution , should be added from a stock
solution just before the lysis buffer is used . The rate of inactivation in aqueous
solution increases with pH and is faster at 25°C than at 4°C . The half - life of a 20
um ...
Page 62
PMSF , which is labile in aqueous solutions , should be added from a stock
solution just before the suspension buffer is used . The rate of inactivation in
aqueous solution increases with pH and is faster at 25°C than at 4°C . The half -
life of a ...
PMSF , which is labile in aqueous solutions , should be added from a stock
solution just before the suspension buffer is used . The rate of inactivation in
aqueous solution increases with pH and is faster at 25°C than at 4°C . The half -
life of a ...
Page 3
The key step , the removal of proteins , can often be carried out simply by
extracting aqueous solutions of nucleic acids with phenol : chloroform and
chloroform . Such extractions are used whenever it is necessary to inactivate and
remove ...
The key step , the removal of proteins , can often be carried out simply by
extracting aqueous solutions of nucleic acids with phenol : chloroform and
chloroform . Such extractions are used whenever it is necessary to inactivate and
remove ...
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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
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
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