Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 57
Page 11-39
Reattach the barrel to the column . ( This is done to prevent air being sucked
back into the column . ) d . Wash out the organic solvent two times with a 10 - ml
aliquot of sterile , filtered H , O ( Milli - Q or equivalent ) . Repeat step c after each
...
Reattach the barrel to the column . ( This is done to prevent air being sucked
back into the column . ) d . Wash out the organic solvent two times with a 10 - ml
aliquot of sterile , filtered H , O ( Milli - Q or equivalent ) . Repeat step c after each
...
Page 11-52
A set of theoretical curves relating the temperature of the washing solution to the
length and homology of the probe is ... The filters are washed extensively in 6 x
SSC at room temperature and then briefly ( 5 - 10 minutes in 6 X SSC ) at the ...
A set of theoretical curves relating the temperature of the washing solution to the
length and homology of the probe is ... The filters are washed extensively in 6 x
SSC at room temperature and then briefly ( 5 - 10 minutes in 6 X SSC ) at the ...
Page 12-19
The antibody solution can be stored at 4°C and reused several times . Sodium
azide ( see Caution above ) should be added to a final concentration of 0 . 05 %
to inhibit the growth of microorganisms . 13 . Wash the filters for 10 minutes in
each ...
The antibody solution can be stored at 4°C and reused several times . Sodium
azide ( see Caution above ) should be added to a final concentration of 0 . 05 %
to inhibit the growth of microorganisms . 13 . Wash the filters for 10 minutes in
each ...
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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
DNA METHYLATION 5 | 8-5 |
SOLUTIONS FOR WORKING WITH BACTERIOPHAGEI A | 8-7 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
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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 isolation 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 vectors volume