Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 12-17
blunt - ended forceps ( e . g . , Millipore forceps ) , remove the filters from the
solution , and allow them to dry at room temperature on a pad of Kimwipes . 00
Nitrocellulose filters that are free of Triton X - 100 ( Millipore HATF or equivalent )
give ...
blunt - ended forceps ( e . g . , Millipore forceps ) , remove the filters from the
solution , and allow them to dry at room temperature on a pad of Kimwipes . 00
Nitrocellulose filters that are free of Triton X - 100 ( Millipore HATF or equivalent )
give ...
Page 12-18
If large areas of the top agarose stick to the nitrocellulose filters , chill the plates
for 30 minutes at 4 ° C or 5 minutes at -20 ° C before peeling off the filters . ...
Remove the lids from the plates 30 minutes before removing the first filter . b .
If large areas of the top agarose stick to the nitrocellulose filters , chill the plates
for 30 minutes at 4 ° C or 5 minutes at -20 ° C before peeling off the filters . ...
Remove the lids from the plates 30 minutes before removing the first filter . b .
Page 12-24
Processing Filters for Immunological Screening of Colonies Caution : Step 1
should be carried out in a chemical hood . 1 . Using blunt - ended forceps ( e . g .
, Millipore forceps ) , remove the nitrocellulose filters from the plates and place
them ...
Processing Filters for Immunological Screening of Colonies Caution : Step 1
should be carried out in a chemical hood . 1 . Using blunt - ended forceps ( e . g .
, Millipore forceps ) , remove the nitrocellulose filters from the plates and place
them ...
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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