Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 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 .
Chill the ...
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 .
Chill the ...
Page 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 ...
Page 34
The filters are then processed and screened as described below . The following
method was provided by S . McKnight . 1 . Remove the nitrocellulose filters from
the lawn of plaques with bluntended forceps ( e . g . , Millipore forceps ) and
place ...
The filters are then processed and screened as described below . The following
method was provided by S . McKnight . 1 . Remove the nitrocellulose filters from
the lawn of plaques with bluntended forceps ( e . g . , Millipore forceps ) and
place ...
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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
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
Copyright | |
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Common terms and phrases
acid activity agarose aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies concentration constructed containing deletions denatured described determine digestion DNA polymerase dNTPs double-stranded efficiency electrophoresis et al ethanol expression Figure filters fragment gene genomic hybridization increase Incubate inserted interest isolated labeled length libraries ligation linear linkers method microfuge minutes mixture molecules mRNA mutagenesis mutagenic mutations Nucleic nucleotides obtained oligonucleotide original plaques plasmid plasmid DNA plate pool position possible prepared presence primer probe problem protein purified radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening sequence single single-stranded solution specific step Store strand synthesis target DNA target sequence template termini tion transfer transformants tube units usually vector volume