Manual of Methods for General Bacteriology |
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Page 22
Special methods for the examination of growing cultures of bacteria were described in Chapter 2. Three commonly used methods for the examination simply of living cells , as needed for usual determinative purposes , are described as ...
Special methods for the examination of growing cultures of bacteria were described in Chapter 2. Three commonly used methods for the examination simply of living cells , as needed for usual determinative purposes , are described as ...
Page 40
However , as of other examination by transmission electron the photographic negatives ( with appropriate microscopy , may be found in references 53-63 . development ) will have more contrast than anticipated while presenting a greater ...
However , as of other examination by transmission electron the photographic negatives ( with appropriate microscopy , may be found in references 53-63 . development ) will have more contrast than anticipated while presenting a greater ...
Page 194
... be asimate rule has been proposed that the dry weight sessed by examination of their blueprints , by concentration is directly proportional to the ab- examination of their optical design , or by comsorbance ( 28 ) .
... be asimate rule has been proposed that the dry weight sessed by examination of their blueprints , by concentration is directly proportional to the ab- examination of their optical design , or by comsorbance ( 28 ) .
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Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York