Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 12
Prepare a column of protein A - Sepharose , equilibrated in 100 mm Tris · Cl ( pH
8 . ... For the preparation of IgG for most laboratory purposes , 1 - ml columns are
poured and run in pasteur pipettes plugged with sterile glass wool . 2 . Add 0 .
Prepare a column of protein A - Sepharose , equilibrated in 100 mm Tris · Cl ( pH
8 . ... For the preparation of IgG for most laboratory purposes , 1 - ml columns are
poured and run in pasteur pipettes plugged with sterile glass wool . 2 . Add 0 .
Page 32
8 ) , whereas doube - stranded DNA is not removed from the column until the
phosphate concentration exceeds 0 . 36 M . 2 . Prepare SS and DS buffers by
diluting 2 m sodium phosphate ( pH 6 . 8 ) . 2 M sodium phosphate ( pH 6 . 8 ) is
made ...
8 ) , whereas doube - stranded DNA is not removed from the column until the
phosphate concentration exceeds 0 . 36 M . 2 . Prepare SS and DS buffers by
diluting 2 m sodium phosphate ( pH 6 . 8 ) . 2 M sodium phosphate ( pH 6 . 8 ) is
made ...
Page 36
Column Chromatography 1 . Sephadex and Bio - Gel columns can be
conveniently prepared in disposable 5 - ml borosilicate glass pipettes or pasteur
pipettes plugged with a small amount of sterile glass wool . Use a long , narrow
pipette ( e ...
Column Chromatography 1 . Sephadex and Bio - Gel columns can be
conveniently prepared in disposable 5 - ml borosilicate glass pipettes or pasteur
pipettes plugged with a small amount of sterile glass wool . Use a long , narrow
pipette ( e ...
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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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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