Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 11-29
Isolation of oligonucleotides by Reversed - phase Chromatography on a Silica
Gel Isolate oligonucleotides from the filtered solution ( step 15 , page 11 . 28 )
either by reversed - phase chromatography on a silica gel as described below or
by ...
Isolation of oligonucleotides by Reversed - phase Chromatography on a Silica
Gel Isolate oligonucleotides from the filtered solution ( step 15 , page 11 . 28 )
either by reversed - phase chromatography on a silica gel as described below or
by ...
Page 13-24
Because the next step of the procedure requires the target DNA to be ligated to
itself , it is best to use restriction enzymes that generate compatible termini . If this
is not possible , an acceptable alternative is to use restriction enzymes that ...
Because the next step of the procedure requires the target DNA to be ligated to
itself , it is best to use restriction enzymes that generate compatible termini . If this
is not possible , an acceptable alternative is to use restriction enzymes that ...
Page 15-25
10 x Polymerase buffer 200 mm Tris . Cl ( pH 7 . 6 ) 10 mM MgCl , 1 mm
dithiothreitol 11 . Purify the DNAs by extraction with phenol : chloroform , and
then precipitate the DNAs with ethanol as described in steps 6 – 8 . Redissolve
each of the ...
10 x Polymerase buffer 200 mm Tris . Cl ( pH 7 . 6 ) 10 mM MgCl , 1 mm
dithiothreitol 11 . Purify the DNAs by extraction with phenol : chloroform , and
then precipitate the DNAs with ethanol as described in steps 6 – 8 . Redissolve
each of the ...
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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