Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 2
Methods for expressing large amounts of protein from a cloned gene introduced
into Escherichia coli have proven invaluable in the purification , localization , and
functional analysis of proteins . For example , fusion proteins consisting of ...
Methods for expressing large amounts of protein from a cloned gene introduced
into Escherichia coli have proven invaluable in the purification , localization , and
functional analysis of proteins . For example , fusion proteins consisting of ...
Page 29
In particular , it may be important that the protein not have an amino - terminal
methionine , which is coded for by the ATG in these vectors . The amino - terminal
methionine is removed in E . coli to different extents for different proteins .
Another ...
In particular , it may be important that the protein not have an amino - terminal
methionine , which is coded for by the ATG in these vectors . The amino - terminal
methionine is removed in E . coli to different extents for different proteins .
Another ...
Page 2
In this chapter , we describe techniques to detect and quantitate foreign proteins
synthesized in these systems . ... In a few cases , the protein of interest carries an
enzymatic or other biological activity ( e . g . , the ability to bind a specific ligand )
...
In this chapter , we describe techniques to detect and quantitate foreign proteins
synthesized in these systems . ... In a few cases , the protein of interest carries an
enzymatic or other biological activity ( e . g . , the ability to bind a specific ligand )
...
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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