Manual of Methods for General Bacteriology |
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Page 198
have been used to measure bacterial concentra - domly distributed in space ,
then light - scattering tions . Instruments designed to make right - angle
measurement over a range of angles can give measurements of light scattering
are called ...
have been used to measure bacterial concentra - domly distributed in space ,
then light - scattering tions . Instruments designed to make right - angle
measurement over a range of angles can give measurements of light scattering
are called ...
Page 287
When I . is set at 100 , the quantity measured directly is percent transmittance ( %
T ) . % T can be related to molar concentration ( C ) of an absorbing solute
through the Beer - Lambert law - log % T = E . L . C = A where e is the molar
extinction ...
When I . is set at 100 , the quantity measured directly is percent transmittance ( %
T ) . % T can be related to molar concentration ( C ) of an absorbing solute
through the Beer - Lambert law - log % T = E . L . C = A where e is the molar
extinction ...
Page 292
Turbidity contributes to error through scatter - ing , which is measured as
fluorescence . Thus , maintenance of scrupulously clean glassware for
measurement and storage of solutions is neces - sary . Many of the above effects
can be ...
Turbidity contributes to error through scatter - ing , which is measured as
fluorescence . Thus , maintenance of scrupulously clean glassware for
measurement and storage of solutions is neces - sary . Many of the above effects
can be ...
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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