Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 9-58
Removal of Radiolabeled Probes from Nitrocellulose Filters and Nylon
Membranes Probes become irreversibly bound if nitrocellulose filters and nylon
... Remove the fluid from the heat and add SDS to a final concentration of 0.1 % .
Immerse ...
Removal of Radiolabeled Probes from Nitrocellulose Filters and Nylon
Membranes Probes become irreversibly bound if nitrocellulose filters and nylon
... Remove the fluid from the heat and add SDS to a final concentration of 0.1 % .
Immerse ...
Page 11-36
Remove the tube from the bath , and allow the mixture to thaw at room
temperature . 4 . Centrifuge at 12 , 000g for 5 minutes at 4°C in a microfuge .
Using a pasteur pipette , carefully remove all of the fluid from the tube . Add 500
ul of distilled H ...
Remove the tube from the bath , and allow the mixture to thaw at room
temperature . 4 . Centrifuge at 12 , 000g for 5 minutes at 4°C in a microfuge .
Using a pasteur pipette , carefully remove all of the fluid from the tube . Add 500
ul of distilled H ...
Page 13-54
Carefully remove the shark's tooth comb from the top of the gel , and strip the
electrical tape from the bottom of the gel mold . This is best done by cutting the
tape into several segments with a scalpel blade and then removing each
segment in ...
Carefully remove the shark's tooth comb from the top of the gel , and strip the
electrical tape from the bottom of the gel mold . This is best done by cutting the
tape into several segments with a scalpel blade and then removing each
segment in ...
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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