Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 77
Page 10-20
Primer : Template Ratios and Nucleotide Concentrations The size , specific
activity , and yield of the radioactive strand synthesized by the Klenow fragment
of E . coli DNA polymerase I are affected by the relative concentrations of primer ...
Primer : Template Ratios and Nucleotide Concentrations The size , specific
activity , and yield of the radioactive strand synthesized by the Klenow fragment
of E . coli DNA polymerase I are affected by the relative concentrations of primer ...
Page 13-76
... primer , radioactive precursor ) omitted from reaction Saran Wrap not removed
from gel after drying No template DNA ... site deleted from template High
concentrations of EDTA present Incorrect primer used One set of sequencing
reactions ...
... primer , radioactive precursor ) omitted from reaction Saran Wrap not removed
from gel after drying No template DNA ... site deleted from template High
concentrations of EDTA present Incorrect primer used One set of sequencing
reactions ...
Page 14-32
ing a narrower range of concentrations of control template . In addition to the
usual ingredients , this series of reactions should contain : incremental dilutions
of control template ( 1 : 10 , 2 : 10 , 3 : 10 , 4 : 10 , etc . ) 10 ul [ a - " P ] DCTP ( sp .
act ...
ing a narrower range of concentrations of control template . In addition to the
usual ingredients , this series of reactions should contain : incremental dilutions
of control template ( 1 : 10 , 2 : 10 , 3 : 10 , 4 : 10 , etc . ) 10 ul [ a - " P ] DCTP ( sp .
act ...
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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