Manual of Methods for General Bacteriology |
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Page 195
However , There is a second reason for adopting a routine the photometric
measurements at this level are timing procedure for measuring cell turbidity , not
accurate ... For such small absorbance measure alignment of rod - shaped
particles .
However , There is a second reason for adopting a routine the photometric
measurements at this level are timing procedure for measuring cell turbidity , not
accurate ... For such small absorbance measure alignment of rod - shaped
particles .
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 292
the use of pure reagents . In addition , errors can The ability to measure a specific
ion is deresult from nonuniform contamination of sam pendent upon the
construction of the measuring ples and glassware by a variety of fluorescent
electrode .
the use of pure reagents . In addition , errors can The ability to measure a specific
ion is deresult from nonuniform contamination of sam pendent upon the
construction of the measuring ples and glassware by a variety of fluorescent
electrode .
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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