Manual of Methods for General Bacteriology |
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Page 167
Selection - synchrony procedure . Delay synchronization experiments until
reproducible batch cultivation conditions can be established , including
determination of asynchronous culture kinetics . When these prerequisites are
met , establish ...
Selection - synchrony procedure . Delay synchronization experiments until
reproducible batch cultivation conditions can be established , including
determination of asynchronous culture kinetics . When these prerequisites are
met , establish ...
Page 229
... in the growth period is too lengthy , the mutant cells same medium before
proceeding to the selection will also undergo duplication , thus leading to the or
screening step . possibility of recovering several replicas of the same mutation .
... in the growth period is too lengthy , the mutant cells same medium before
proceeding to the selection will also undergo duplication , thus leading to the or
screening step . possibility of recovering several replicas of the same mutation .
Page 444
STRAIN SELECTION . . . . 21 . 2 . TEST SELECTION 21 . 3 . DATA CODING 21 . 4
. COMPUTER ANALYSIS 21 . 5 . PRESENTATION AND INTERPRETATION OF
RESULTS 21 . 6 . LITERATURE CITED 21 . 6 . 1 . General References .
STRAIN SELECTION . . . . 21 . 2 . TEST SELECTION 21 . 3 . DATA CODING 21 . 4
. COMPUTER ANALYSIS 21 . 5 . PRESENTATION AND INTERPRETATION OF
RESULTS 21 . 6 . LITERATURE CITED 21 . 6 . 1 . General References .
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Contents
55 | 32 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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absorbance acid activity added addition Adjust agar allow amino acids amount anaerobic applications appropriate assay autoclaving bacteria Bacteriol base broth buffer cells centrifuge colonies column components compounds concentration containing counting cover culture described determine dilution Dissolve distilled water effective electron enrichment enzyme examine example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter microscopy mixture mutants obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts sample selection separation slide sodium solution specific staining standard sterile substrate surface suspension Table techniques temperature tion transfer tube usually values vitamin volume Wash York