Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 34
28 ) , followed by SDS - polyacrylamide gel electrophoresis and autoradiography
, may allow detection of the protein of interest . 2 . ... In addition , sometimes
proteins that are not detectable in Laemmli gels are detected by western gels . 3 .
28 ) , followed by SDS - polyacrylamide gel electrophoresis and autoradiography
, may allow detection of the protein of interest . 2 . ... In addition , sometimes
proteins that are not detectable in Laemmli gels are detected by western gels . 3 .
Page 2
In this chapter , we describe techniques to detect and quantitate foreign proteins
synthesized in these systems . ... Proteins synthesized in heterologous systems
can be detected either by assaying for a particular biological activity or by ...
In this chapter , we describe techniques to detect and quantitate foreign proteins
synthesized in these systems . ... Proteins synthesized in heterologous systems
can be detected either by assaying for a particular biological activity or by ...
Page 63
If possible , calculate the amount of sample that will be required to detect the
target protein by western blotting . The lowest amount of an average - sized
protein that can be detected by western blotting is approximately 1 - 5 ng .
Approximately ...
If possible , calculate the amount of sample that will be required to detect the
target protein by western blotting . The lowest amount of an average - sized
protein that can be detected by western blotting is approximately 1 - 5 ng .
Approximately ...
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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
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