Molecular Cloning: A Laboratory Manual, Book 3 |
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Page vii
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. Identification
of Bacterial Colonies That Contain Recombinant Plasmids 1 . 85 RESTRICTION
ANALYSIS OF SMALL - SCALE PREPARATIONS OF PLASMID DNA 1 .
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. Identification
of Bacterial Colonies That Contain Recombinant Plasmids 1 . 85 RESTRICTION
ANALYSIS OF SMALL - SCALE PREPARATIONS OF PLASMID DNA 1 .
Page 36
Individual colonies may be cloned and propagated for assay ( for methods , see
Jakoby and Pastan 1979 ) . A permanent record of the numbers of colonies may
be obtained by fixing the remaining cells with ice - cold methanol for 15 minutes ...
Individual colonies may be cloned and propagated for assay ( for methods , see
Jakoby and Pastan 1979 ) . A permanent record of the numbers of colonies may
be obtained by fixing the remaining cells with ice - cold methanol for 15 minutes ...
Page 8
Test individual colonies for the presence of the desired insert by plasmid
minipreps . If most of the colonies can be assumed to contain a cDNA ( because
directional cloning or a dephosphorylated vector was used in step 1 ) , they can
be ...
Test individual colonies for the presence of the desired insert by plasmid
minipreps . If most of the colonies can be assumed to contain a cDNA ( because
directional cloning or a dephosphorylated vector was used in step 1 ) , they can
be ...
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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