Manual of Methods for General Bacteriology |
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Page 115
Another approach is to add some of the sam - ple in which spores are suspected
to a suitable growth medium , heat at 80°C for 10 min , and then incubate the
broth for a day or so to permit growth to occur before streaking the culture onto
solid ...
Another approach is to add some of the sam - ple in which spores are suspected
to a suitable growth medium , heat at 80°C for 10 min , and then incubate the
broth for a day or so to permit growth to occur before streaking the culture onto
solid ...
Page 477
Biological indicators ( BIS ) contain known concentrations of microorganisms ,
usually bacterial spores , which exhibit a predictable death rate when exposed to
a defined treatment . BIs may be prepared on various adventitious substrates ( e
...
Biological indicators ( BIS ) contain known concentrations of microorganisms ,
usually bacterial spores , which exhibit a predictable death rate when exposed to
a defined treatment . BIs may be prepared on various adventitious substrates ( e
...
Page 478
6 ) Moist heat Parenteral solutions Spore strip contain American Biological
ConInstruments ing one species of trol Co . Aseptic process equipment bacterium
American Sterilizer Co . Culture media BBL Microbiology Systems Rubber
stoppers ...
6 ) Moist heat Parenteral solutions Spore strip contain American Biological
ConInstruments ing one species of trol Co . Aseptic process equipment bacterium
American Sterilizer Co . Culture media BBL Microbiology Systems Rubber
stoppers ...
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Contents
55 | 32 |
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 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 enrichment 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 mg/liter microscopy mixture mutants 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