Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 24
Partial Digestion of High - molecular - weight Eukaryotic DNA with Restriction
Enzymes The only method by which DNA can be fragmented in truly random
fashion , irrespective of its base composition and sequence , is mechanical
shearing .
Partial Digestion of High - molecular - weight Eukaryotic DNA with Restriction
Enzymes The only method by which DNA can be fragmented in truly random
fashion , irrespective of its base composition and sequence , is mechanical
shearing .
Page 32
After digestion is complete , the fragments of DNA are concentrated by
precipitation with ethanol and are applied to the gel ... The chief problem
encountered during digestion of high - molecular - weight DNA is unevenness of
digestion caused ...
After digestion is complete , the fragments of DNA are concentrated by
precipitation with ethanol and are applied to the gel ... The chief problem
encountered during digestion of high - molecular - weight DNA is unevenness of
digestion caused ...
Page 21
Sonication and digestion with DNAase I are superior to digestion with restriction
enzymes in a number respects . ... Second , both methods yield a collection of
overlapping fragmentssomething that is impossible when DNA is digested to ...
Sonication and digestion with DNAase I are superior to digestion with restriction
enzymes in a number respects . ... Second , both methods yield a collection of
overlapping fragmentssomething that is impossible when DNA is digested to ...
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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
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
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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