Manual of Methods for General Bacteriology |
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Page 187
Finally , in closed containers the plates do not dry out and can be used to look for slow- or late - developing colonies . Another point of concern has to do with CO2 . Even organisms not usually isolated in a high CO2 atmosphere may ...
Finally , in closed containers the plates do not dry out and can be used to look for slow- or late - developing colonies . Another point of concern has to do with CO2 . Even organisms not usually isolated in a high CO2 atmosphere may ...
Page 232
A tected as white colonies while the lactose - negapartial revertant strain may produce an enzyme tive variants are bright red . The basis for this of very low specific activity , but as a result of differential staining is that lactose ...
A tected as white colonies while the lactose - negapartial revertant strain may produce an enzyme tive variants are bright red . The basis for this of very low specific activity , but as a result of differential staining is that lactose ...
Page 233
Also see transfer of a large number of colonies from one 20.2.5 . plating medium to another in a single operation Procedure . by use of cotton velveteen cloth ( 13.9.16 ) . Furthermore , the exact pattern of colonies on the 1.
Also see transfer of a large number of colonies from one 20.2.5 . plating medium to another in a single operation Procedure . by use of cotton velveteen cloth ( 13.9.16 ) . Furthermore , the exact pattern of colonies on the 1.
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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