Manual of Methods for General Bacteriology |
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Page 67
Indicator solutions and papers , and their corre - sponding color standards for
various pH ranges , are available from ... Select the appropriate indicator for the
pH range of interest , and make sure that it does not inhibit growth of the
organism .
Indicator solutions and papers , and their corre - sponding color standards for
various pH ranges , are available from ... Select the appropriate indicator for the
pH range of interest , and make sure that it does not inhibit growth of the
organism .
Page 70
A statistical analysis ( 34 ) of measurements made with the electronic Sina -
Scope instrument ( over the range of 0 . 755 to 0 . 967 aw ) indicated a variation
of less than + 0 . 01 . The most commonly used instruments for measuring
osmotic ...
A statistical analysis ( 34 ) of measurements made with the electronic Sina -
Scope instrument ( over the range of 0 . 755 to 0 . 967 aw ) indicated a variation
of less than + 0 . 01 . The most commonly used instruments for measuring
osmotic ...
Page 198
Instruments designed to make right - angle measurement over a range of angles
can give measurements of light scattering are called information about : the state
of aggregation of nephelometers . Bacterial concentration may be the ...
Instruments designed to make right - angle measurement over a range of angles
can give measurements of light scattering are called information about : the state
of aggregation of nephelometers . Bacterial concentration may be the ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
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 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 Microbiol microscopy mixture mutants needed 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