Molecular Cloning: A Laboratory Manual, Book 3 |
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Results 1-3 of 62
Page 21
Quantitative results can be obtained only when the amount of antigen bound to
the first antibody is proportional to its concentration in the sample being tested .
To compare the amount of antigen in a number of test samples , assay several ...
Quantitative results can be obtained only when the amount of antigen bound to
the first antibody is proportional to its concentration in the sample being tested .
To compare the amount of antigen in a number of test samples , assay several ...
Page 63
The sample should become highly viscous as a consequence of the release of
highmolecular - weight chromosomal DNA . ... a sonicator with an immersible tip
or a sonicator that can process several samples simultaneously in a chilled cup .
The sample should become highly viscous as a consequence of the release of
highmolecular - weight chromosomal DNA . ... a sonicator with an immersible tip
or a sonicator that can process several samples simultaneously in a chilled cup .
Page 5
If the sample is pure ( i . e . , without significant amounts of contaminants such as
proteins , phenol , agarose , or other nucleic acids ) , spectrophotometric
measurement of the amount of ultraviolet irradiation absorbed by the bases is
simple ...
If the sample is pure ( i . e . , without significant amounts of contaminants such as
proteins , phenol , agarose , or other nucleic acids ) , spectrophotometric
measurement of the amount of ultraviolet irradiation absorbed by the bases is
simple ...
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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
Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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Common terms and phrases
acetate activity added Adjust aliquots allow amount antibody antigen Appendix appropriate approximately aqueous assay bacterial bacteriophage base binding buffer carried cells centrifugation Chapter chromatography Cl pH cloned coli column complete concentration containing culture deionized water described desired detected dilution Dissolve EDTA efficiency electrophoresis enzyme et al ethanol expression extract Figure filter final fragment gene growth hybridization Incubate levels ligation mammalian cells medium method mg/ml microfuge tube minutes mixture mRNAs nucleic acid pellet phase phosphate Place plasmid plate polymerase precipitation prepared procedure Products promoter protein radioactive radiolabeled reaction remove restriction room temperature sample screen selection sequence sodium solution specific step sterile stored strain TABLE Telephone termini tion transcription transfection transfer transformation Tris ug/ml usually vectors volume wash western blotting ОН