Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 79
Page 9-27
26 ) , digest 100 ug of high - molecular - weight DNA with the appropriate amount
of restriction enzyme for the appropriate time . To ensure that the conditions for
the large - scale digestion are as identical as possible to those used in the pilot ...
26 ) , digest 100 ug of high - molecular - weight DNA with the appropriate amount
of restriction enzyme for the appropriate time . To ensure that the conditions for
the large - scale digestion are as identical as possible to those used in the pilot ...
Page 15-25
To each DNA , add 2 ul of the appropriate 10 x restriction enzyme buffer and 8
units of a restriction enzyme that will separate the target DNA from the vector .
Incubate the reactions for 1 hour at the appropriate temperature . 13 . At the end
of the ...
To each DNA , add 2 ul of the appropriate 10 x restriction enzyme buffer and 8
units of a restriction enzyme that will separate the target DNA from the vector .
Incubate the reactions for 1 hour at the appropriate temperature . 13 . At the end
of the ...
Page 15-30
6 ) 22 ul the appropriate 10 x restriction enzyme buffer 5 ul the appropriate
restriction enzyme 5 - 10 units Incubate the reaction for 2 hours at the appropriate
temperature . 16 . Transform ( plasmids or phagemids ) or transfect (
bacteriophage ...
6 ) 22 ul the appropriate 10 x restriction enzyme buffer 5 ul the appropriate
restriction enzyme 5 - 10 units Incubate the reaction for 2 hours at the appropriate
temperature . 16 . Transform ( plasmids or phagemids ) or transfect (
bacteriophage ...
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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