Manual of Methods for General Bacteriology |
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Page 67
Possible inhibitory or toxic effects of the solutions or paper . By proper selection of either , buffer . the pH can be estimated within 20.2 pH unit . 3. Possible utilization of the buffer by the Indicator solutions and papers ...
Possible inhibitory or toxic effects of the solutions or paper . By proper selection of either , buffer . the pH can be estimated within 20.2 pH unit . 3. Possible utilization of the buffer by the Indicator solutions and papers ...
Page 256
It Generalized transducing phages are known for has also been possible to use P1 - mediated transa variety of bacterial genera . Probably the best duction to construct strains of desired genotypes . studied system makes use of phage P22 ...
It Generalized transducing phages are known for has also been possible to use P1 - mediated transa variety of bacterial genera . Probably the best duction to construct strains of desired genotypes . studied system makes use of phage P22 ...
Page 398
The common clip - on funnel attachment It is possible sometimes to avoid the problems for the filter unit may be replaced with a customof washing cells by centrifuging them through a made heavy brass ring to hold down the filter layer ...
The common clip - on funnel attachment It is possible sometimes to avoid the problems for the filter unit may be replaced with a customof washing cells by centrifuging them through a made heavy brass ring to hold down the filter layer ...
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Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York