Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 38
Prepare the solutions and form the calcium phosphate - DNA coprecipitate . as
described on pages 16 . 33 – 16 . 34 , steps 1 and 3 . 2 . While the precipitate is
forming , collect the exponentially growing cells by centrifugation at 800g for 5 ...
Prepare the solutions and form the calcium phosphate - DNA coprecipitate . as
described on pages 16 . 33 – 16 . 34 , steps 1 and 3 . 2 . While the precipitate is
forming , collect the exponentially growing cells by centrifugation at 800g for 5 ...
Page 25
PKK240 - 11 provides a tac promoter and a lacZ ribosomebinding site . 2 . If
necessary , cleave the vector with a restriction enzyme that cuts at a downstream
site compatible with the DNA fragment prepared by one of the methods described
...
PKK240 - 11 provides a tac promoter and a lacZ ribosomebinding site . 2 . If
necessary , cleave the vector with a restriction enzyme that cuts at a downstream
site compatible with the DNA fragment prepared by one of the methods described
...
Page 80
Relevant immunoprecipitation techniques are described on pages 18 . 44 – 18 .
46 , and detailed and standardized procedures for electrophoresis in SDS -
polyacrylamide gels are described on pages 18 . 47 – 18 . 54 . Notes i . For
analysis ...
Relevant immunoprecipitation techniques are described on pages 18 . 44 – 18 .
46 , and detailed and standardized procedures for electrophoresis in SDS -
polyacrylamide gels are described on pages 18 . 47 – 18 . 54 . Notes i . For
analysis ...
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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
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