Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 32
0 ul bacteriophage T4 polynucleotide kinase ( 8 units / ul ) 2 . 0 ul Incubate the
reactions for 1 hour ... Most manufacturers ( apart from New England Biolabs )
now calibrate the enzyme in Weiss units ( Weiss et al . 1968 ) . One Weiss unit is
the ...
0 ul bacteriophage T4 polynucleotide kinase ( 8 units / ul ) 2 . 0 ul Incubate the
reactions for 1 hour ... Most manufacturers ( apart from New England Biolabs )
now calibrate the enzyme in Weiss units ( Weiss et al . 1968 ) . One Weiss unit is
the ...
Page 11
e exchange of Weiss unit corresponds 1970 ) and to At least three different
assays are used to measure the activity of ... Most manufacturers ( apart from
New England Biolabs ) now calibrate the enzyme in Weiss units ( Weiss et al .
1968 ) .
e exchange of Weiss unit corresponds 1970 ) and to At least three different
assays are used to measure the activity of ... Most manufacturers ( apart from
New England Biolabs ) now calibrate the enzyme in Weiss units ( Weiss et al .
1968 ) .
Page 30
Most manufacturers ( apart from New England Biolabs ) now calibrate the
enzyme in Weiss units ( Weiss et al . 1968 ) . One Weiss unit is the amount of
enzyme that catalyzes the exchange of 1 nmole of " PP from pyrophosphate into (
y , B ...
Most manufacturers ( apart from New England Biolabs ) now calibrate the
enzyme in Weiss units ( Weiss et al . 1968 ) . One Weiss unit is the amount of
enzyme that catalyzes the exchange of 1 nmole of " PP from pyrophosphate into (
y , B ...
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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