Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 85
Page 10-51
Labeling the 5 ' and 3 ' Termini of DNA The termini of DNA molecules can be
radiolabeled enzymatically to yield molecules that may be used in nuclease - S1
mapping of RNA , as radiolabeled primers in primer - extension reactions , and
as ...
Labeling the 5 ' and 3 ' Termini of DNA The termini of DNA molecules can be
radiolabeled enzymatically to yield molecules that may be used in nuclease - S1
mapping of RNA , as radiolabeled primers in primer - extension reactions , and
as ...
Page 13-24
Because the next step of the procedure requires the target DNA to be ligated to
itself , it is best to use restriction enzymes that generate compatible termini . If this
is not possible , an acceptable alternative is to use restriction enzymes that ...
Because the next step of the procedure requires the target DNA to be ligated to
itself , it is best to use restriction enzymes that generate compatible termini . If this
is not possible , an acceptable alternative is to use restriction enzymes that ...
Page 13-78
The target DNA can be of any length and can be radiolabeled in a number of
ways , depending on the nature of the termini of the DNA . Asymmetric Labeling
of Target DNA Double - stranded DNA can be labeled in the following ways : • At
its 5 ...
The target DNA can be of any length and can be radiolabeled in a number of
ways , depending on the nature of the termini of the DNA . Asymmetric Labeling
of Target DNA Double - stranded DNA can be labeled in the following ways : • At
its 5 ...
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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