Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 31
Some proteins that are inactive when produced intracellularly are active when
secreted ; secretion may allow them to be properly folded ( Gray et al . 1985 ) .
Proteins are produced that do not have an amino - terminal methionine , since ...
Some proteins that are inactive when produced intracellularly are active when
secreted ; secretion may allow them to be properly folded ( Gray et al . 1985 ) .
Proteins are produced that do not have an amino - terminal methionine , since ...
Page 34
QUANTITATING THE LEVELS OF EXPRESSION OF CLONED GENES After
plasmids containing the transcription and translation initiation signals that allow
the protein of interest to be expressed in E . coli are constructed , the amount of ...
QUANTITATING THE LEVELS OF EXPRESSION OF CLONED GENES After
plasmids containing the transcription and translation initiation signals that allow
the protein of interest to be expressed in E . coli are constructed , the amount of ...
Page 21
Although this is sufficient to allow the emitted ß particles to interact productively
with silver halide crystals in the emulsion , it is not enough to allow the particles to
pass through barriers ( e . g . , Saran Wrap ) that might be placed between the ...
Although this is sufficient to allow the emitted ß particles to interact productively
with silver halide crystals in the emulsion , it is not enough to allow the particles to
pass through barriers ( e . g . , Saran Wrap ) that might be placed between the ...
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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