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
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Common terms and phrases
activity addition aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleavage cleaved clones complete concentration constructed containing deletions denatured described determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filter four fragment gene genomic DNA hybridization increase Incubate inserted interest isolation Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutations nucleic acids nucleotides obtained oligonucleotide original 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 specific step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume