Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 78
Page 8-61
An alternative procedure to monitor synthesis of the first strand of cDNA is to use
a small amount of [ a - 8P ] DCTP ( 10 uCi total ) in the large - scale reaction
described above and a much greater amount ( 100 uCi total ) of radiolabeled
dNTP ...
An alternative procedure to monitor synthesis of the first strand of cDNA is to use
a small amount of [ a - 8P ] DCTP ( 10 uCi total ) in the large - scale reaction
described above and a much greater amount ( 100 uCi total ) of radiolabeled
dNTP ...
Page 8-73
In these reactions , a constant amount of bacteriophage d arms is ligated to
varying amounts of cDNA . The aim is to determine the amount of cDNA that
yields at least 5 x 10° recombinant bacteriophages ( i . e . , a mammalian cDNA
library of ...
In these reactions , a constant amount of bacteriophage d arms is ligated to
varying amounts of cDNA . The aim is to determine the amount of cDNA that
yields at least 5 x 10° recombinant bacteriophages ( i . e . , a mammalian cDNA
library of ...
Page 10-9
a - 32P and three unlabeled dNTPs or to dilute each [ a - 32P ] dNTP with an
appropriate amount of the unlabeled dNTP . Most commercial suppliers sell [ a -
32P ] dNTPs in a concentrated aqueous solution , which can be added directly to
the ...
a - 32P and three unlabeled dNTPs or to dilute each [ a - 32P ] dNTP with an
appropriate amount of the unlabeled dNTP . Most commercial suppliers sell [ a -
32P ] dNTPs in a concentrated aqueous solution , which can be added directly to
the ...
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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
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Common terms and phrases
activity addition aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleavage cleaved clones complete concentration constructed containing deletions denatured described determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filter four fragment gene genomic DNA hybridization increase Incubate inserted interest isolation Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutations nucleic acids nucleotides obtained oligonucleotide original 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 specific step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume