Manual of Methods for General Bacteriology |
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Page 238
The S - 9 mix is freshly prepared each day cases , the compounds can be spotted directly on and may be kept for several ... Procedure for preparation of test comCAUTION : The test organism , S. typhimupounds . rium , is a class II human ...
The S - 9 mix is freshly prepared each day cases , the compounds can be spotted directly on and may be kept for several ... Procedure for preparation of test comCAUTION : The test organism , S. typhimupounds . rium , is a class II human ...
Page 264
Alternatively , stock solutions can be prepared and stored at -20 ° C . Corrections should be made for buffers or other ingredients to achieve the correct concentration of pure ampicillin . Suspended in 50 % ethanol and stored at 4 ° C ...
Alternatively , stock solutions can be prepared and stored at -20 ° C . Corrections should be made for buffers or other ingredients to achieve the correct concentration of pure ampicillin . Suspended in 50 % ethanol and stored at 4 ° C ...
Page 334
Commercial glucose oxidase - peroxidase preparation : Prepare the dry enzyme mixture according to the manufacturer's instructions . Chromogen : Available as part of the commercial kits . Prepare according to the manufacturer's ...
Commercial glucose oxidase - peroxidase preparation : Prepare the dry enzyme mixture according to the manufacturer's instructions . Chromogen : Available as part of the commercial kits . Prepare according to the manufacturer's ...
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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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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