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EXPERIMENTAL PROCEDURES AND RESULTS 1249
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30 minutes 53-20 was infected abortive infection adsorbed adsorption Adsorption was allowed aeration agar allowed to proceed antiserum approximately bacterial bacterium CARBON DIOXIDE EVOLUTION cells of ML chloroform coli CONTROL O Nl culture ML CULTURES OF ML digestion diluted distilled water DNA DETERMINATIONS enzymes extracts fected cells FIGURE flasks genetic grams increase incubated Infected Cultures infected v/ith infected with Nl INFECTED X N6 infection of ML infective centers intervals latter Lowry Protein Assay lysates lysed lysis lysodeikticus lysozyme mixed ML 53-20 infected ml aliquots N6 Infected Nl N6 phage N6 type nitrogen Nl and N6 OPTICAL DENSITIES particles per ml phage maturation phage when infected plaques when plated plated with ML prepared produce plaques progeny Reagent recombination recovery of infective ribonucleic acid sample seeded with ML Servall Simultaneous infection soft agar solution strain supernatant test tubes titer turbidity UNINFECTED AND INFECTED UNINFECTED CONTROL wore