Molecular Cloning: A Laboratory Manual, Book 3 |
From inside the book
Results 1-3 of 69
Page 13
Dissolve 408 . 1 g of sodium acetate . 31 , 0 in 800 ml of 1 , 0 . Adjust the pH to 5 .
2 with glacial acetic acid or adjust the pH to 7 . 0 with dilute acetic acid . Adjust
the volume to 1 liter with H , 0 . Dispense into aliquots and sterilize by autoclaving
...
Dissolve 408 . 1 g of sodium acetate . 31 , 0 in 800 ml of 1 , 0 . Adjust the pH to 5 .
2 with glacial acetic acid or adjust the pH to 7 . 0 with dilute acetic acid . Adjust
the volume to 1 liter with H , 0 . Dispense into aliquots and sterilize by autoclaving
...
Page 8
To the resulting solution , add 0 . 2 volume of fresh 5 % hypophosphorous acid
and 0 . 12 volume of fresh 0 . 5 m sodium nitrite . Mix carefully . Important : Check
that the pH of the solution is < 3 . 0 . Hypophosphorous acid is usually supplied
as ...
To the resulting solution , add 0 . 2 volume of fresh 5 % hypophosphorous acid
and 0 . 12 volume of fresh 0 . 5 m sodium nitrite . Mix carefully . Important : Check
that the pH of the solution is < 3 . 0 . Hypophosphorous acid is usually supplied
as ...
Page 16
By carrying out several cycles of extraction , the volume of a nucleic acid solution
can be reduced significantly . This method of concentration is used to reduce the
volume of dilute solutions to the point where the nucleic acid can easily be ...
By carrying out several cycles of extraction , the volume of a nucleic acid solution
can be reduced significantly . This method of concentration is used to reduce the
volume of dilute solutions to the point where the nucleic acid can easily be ...
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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