Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 58
Removal of Radiolabeled Probes from Nitrocellulose Filters and Nylon
Membranes Probes become irreversibly bound if nitrocellulose filters and nylon
membranes ... Remove the fluid from the heat and add SDS to a final
concentration of 0 .
Removal of Radiolabeled Probes from Nitrocellulose Filters and Nylon
Membranes Probes become irreversibly bound if nitrocellulose filters and nylon
membranes ... Remove the fluid from the heat and add SDS to a final
concentration of 0 .
Page 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 ...
Page 86
Remove the supernatant upernatant . Remove the supernatant carefully and
dispose of carefully and dispose of it in the appropriate it in the appropriate waste
bottle . waste bottle . Add 30 ul hydrazine and mix gently . Incubate 5 minutes at ...
Remove the supernatant upernatant . Remove the supernatant carefully and
dispose of carefully and dispose of it in the appropriate it in the appropriate waste
bottle . waste bottle . Add 30 ul hydrazine and mix gently . Incubate 5 minutes at ...
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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