Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 66
1 m sodium phosphate ( pH 7 . 5 ) 201 ul 100x Mg solution is 0 . 1 M MgCl , , 4 . 5
M B - mercaptoethanol . 1 x ONPG is a 4 mg / ml solution of ONPG dissolved in 0
. 1 m sodium phosphate ( pH 7 . 5 ) . 0 . 1 m Sodium phosphate is made ...
1 m sodium phosphate ( pH 7 . 5 ) 201 ul 100x Mg solution is 0 . 1 M MgCl , , 4 . 5
M B - mercaptoethanol . 1 x ONPG is a 4 mg / ml solution of ONPG dissolved in 0
. 1 m sodium phosphate ( pH 7 . 5 ) . 0 . 1 m Sodium phosphate is made ...
Page 32
Determine the concentrations of sodium phosphate that are optimal for elution of
single - stranded DNA ( SS buffer ) and double - stranded DNA ( DS buffer ) as
described on page E . 30 . Usually , single - stranded DNA elutes in 0 . 14 - 0 .
Determine the concentrations of sodium phosphate that are optimal for elution of
single - stranded DNA ( SS buffer ) and double - stranded DNA ( DS buffer ) as
described on page E . 30 . Usually , single - stranded DNA elutes in 0 . 14 - 0 .
Page 42
Sodium bicarbonate , pH values of stock solutions , B . 3 Sodium bisulfite
mutagenesis of DNA , 15 . 106 Sodium butyrate increases efficiency of
mammalian cell transfection , 16 . 32 , 16 . 35 Sodium carbonate , pH values of
stock solutions , B ...
Sodium bicarbonate , pH values of stock solutions , B . 3 Sodium bisulfite
mutagenesis of DNA , 15 . 106 Sodium butyrate increases efficiency of
mammalian cell transfection , 16 . 32 , 16 . 35 Sodium carbonate , pH values of
stock solutions , B ...
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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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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