Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 8-59
If possible , obtain linkers that are at least 4 - 8 nucleotides longer than the site
recognized by the restriction enzyme . Many restriction enzymes inefficiently
cleave recognition sites located very close to the ends of DNA molecules . 0 . 01
m Tris ...
If possible , obtain linkers that are at least 4 - 8 nucleotides longer than the site
recognized by the restriction enzyme . Many restriction enzymes inefficiently
cleave recognition sites located very close to the ends of DNA molecules . 0 . 01
m Tris ...
Page 8-68
Add : 5x bacteriophage T4 DNA polymerase repair buffer mixture of dNTPs ( 5
mm each ) H2O to a final volume of 50 ul 10 ul 5 ul 5x Bacteriophage T4 DNA
polymerase repair buffer 90 mm ( NH4 ) 2SO4 0.33 m Tris · Cl ( pH 8.3 ) 33 mm ...
Add : 5x bacteriophage T4 DNA polymerase repair buffer mixture of dNTPs ( 5
mm each ) H2O to a final volume of 50 ul 10 ul 5 ul 5x Bacteriophage T4 DNA
polymerase repair buffer 90 mm ( NH4 ) 2SO4 0.33 m Tris · Cl ( pH 8.3 ) 33 mm ...
Page 11-35
0.5 m EDTA - Tris ( pH 6.0 ) Add 0.1 mole of EDTA ( free acid m.w. = 292.2 ) to 60
ml of 1,0 . While stirring the solution , slowly add Tris base ( powder ) until the pH
of the solution reaches 6.0 . By this stage , the concentration of Tris will be ...
0.5 m EDTA - Tris ( pH 6.0 ) Add 0.1 mole of EDTA ( free acid m.w. = 292.2 ) to 60
ml of 1,0 . While stirring the solution , slowly add Tris base ( powder ) until the pH
of the solution reaches 6.0 . By this stage , the concentration of Tris will 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
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
CONCENTRATING NUCLEIC ACIDS E | 8-10 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
MEASUREMENT OF RADIOACTIVITY IN NUCLEIC ACIDS E | 8-18 |
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Common terms and phrases
aliquots allow amount amplification antibody appropriate approximately bacteriophage bacteriophage T4 base binding buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies complete concentration constructed containing deletions denatured described detection determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filters four fragment gene genomic DNA hybridization increase Incubate inserted interest isolated Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutants nucleic acids nucleotides obtained oligonucleotide plaques plasmid DNA plate position possible precipitation prepared presence primer probe problem protein purified radioactivity radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening separate sequence single single-stranded solution step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume