Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 76
Page 10-22
Heat the mixture to 85°C for 5 minutes and then let it cool slowly to 37°C . This
can be achieved by floating the tube in a piece of Styrofoam in a 250 - ml beaker
filled with water equilibrated to 85°C . Store the beaker at room temperature until
...
Heat the mixture to 85°C for 5 minutes and then let it cool slowly to 37°C . This
can be achieved by floating the tube in a piece of Styrofoam in a 250 - ml beaker
filled with water equilibrated to 85°C . Store the beaker at room temperature until
...
Page 11-36
Add 5 - 10 volumes of the EDTA - Tris - DNA solution to a microfuge tube
containing the solution of radiolabeled oligonucleotide that is to be precipitated .
Mix well . For precipitation to be efficient , it is important that the ionic composition
of the ...
Add 5 - 10 volumes of the EDTA - Tris - DNA solution to a microfuge tube
containing the solution of radiolabeled oligonucleotide that is to be precipitated .
Mix well . For precipitation to be efficient , it is important that the ionic composition
of the ...
Page 14-26
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. ANNEALING
1 . In a sterile microfuge tube , mix : 32P - labeled oligonucleotide ( 5 pmoles / ul )
amplified DNA 10 x annealing buffer H2O 1 . 0 ul 10 . 0 ul 1 . 5 ul 2 . 5 ul 10 X ...
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. ANNEALING
1 . In a sterile microfuge tube , mix : 32P - labeled oligonucleotide ( 5 pmoles / ul )
amplified DNA 10 x annealing buffer H2O 1 . 0 ul 10 . 0 ul 1 . 5 ul 2 . 5 ul 10 X ...
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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