Molecular Cloning: A Laboratory Manual, Book 2 |
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Results 1-3 of 81
Page 10-54
DA 3 In many cases , a single buffer ( given below ) can be used both for the
cleavage of DNA with a restriction enzyme and for the subsequent endlabeling .
However , not all restriction enzymes work in bacteriophage T4 DNA polymerase
...
DA 3 In many cases , a single buffer ( given below ) can be used both for the
cleavage of DNA with a restriction enzyme and for the subsequent endlabeling .
However , not all restriction enzymes work in bacteriophage T4 DNA polymerase
...
Page 12-18
When all of the filters have been transferred , agitate the buffer gently for a further
30 minutes at room temperature . If necessary , the filters may be removed from
the buffer at this stage , wrapped in Saran Wrap , and stored for up to 24 hours at
...
When all of the filters have been transferred , agitate the buffer gently for a further
30 minutes at room temperature . If necessary , the filters may be removed from
the buffer at this stage , wrapped in Saran Wrap , and stored for up to 24 hours at
...
Page 12-19
Wash the filters for 10 minutes in each of the buffers below in the order given .
Transfer the filters individually from one buffer to the next . Use 7 . 5 ml of each
buffer for each 82 - mm filter and 15 ml for each 138 - mm filter . TNT + 0 . 1 %
bovine ...
Wash the filters for 10 minutes in each of the buffers below in the order given .
Transfer the filters individually from one buffer to the next . Use 7 . 5 ml of each
buffer for each 82 - mm filter and 15 ml for each 138 - mm filter . TNT + 0 . 1 %
bovine ...
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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