Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 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 in ...
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 in ...
Page 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 9
P and three unlabeled dNTPs or to dilute each [ a - " P ] dNTP with an appropriate
amount of the unlabeled dNTP . Most commercial suppliers sell [ a - " P ] dNTPs
in a concentrated aqueous solution , which can be added directly to the nick ...
P and three unlabeled dNTPs or to dilute each [ a - " P ] dNTP with an appropriate
amount of the unlabeled dNTP . Most commercial suppliers sell [ a - " P ] dNTPs
in a concentrated aqueous solution , which can be added directly to the nick ...
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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 |
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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