Manual of Methods for General Bacteriology |
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Page 161
Operation of the chemostat at dilution rates where D is the dilution rate ( D = F / V
) , So and above Dc will result in complete wash - out of the S are the limiting
substrate concentrations in culture . the feed and fermentor , respectively , u is the
...
Operation of the chemostat at dilution rates where D is the dilution rate ( D = F / V
) , So and above Dc will result in complete wash - out of the S are the limiting
substrate concentrations in culture . the feed and fermentor , respectively , u is the
...
Page 189
Thirdly , if other organisms not of veloped to combine data from different dilution
interest are present in the sample and no ... cultures at each of three successive
contaminating organisms may overgrow the cul 10 - fold dilutions are employed .
Thirdly , if other organisms not of veloped to combine data from different dilution
interest are present in the sample and no ... cultures at each of three successive
contaminating organisms may overgrow the cul 10 - fold dilutions are employed .
Page 431
The working dilution of the antiserum is one - half of the highest dilution that gives
4+ fluorescence . For example , if a 1:20 dilution of the serum is the highest
dilution that gives 4+ fluorescence , the working dilution would be 1:10 .
The working dilution of the antiserum is one - half of the highest dilution that gives
4+ fluorescence . For example , if a 1:20 dilution of the serum is the highest
dilution that gives 4+ fluorescence , the working dilution would be 1:10 .
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Contents
MORPHOLOGY | 5 |
Specimen Preparation for Light Microscopy R G E MURRAY AND C F ROBI | 17 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
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 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 Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plate positive prepared present Press procedure protein reaction reagent references remove 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