Manual of Methods for General Bacteriology |
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Page 73
Therefore , no specific tolerances for Eh can be set for various anaerobic bacteria . However , in standard media , most anaerobic bacteria are inhibited at Eh values higher than - 100 mV . Some will not initiate growth at potentials ...
Therefore , no specific tolerances for Eh can be set for various anaerobic bacteria . However , in standard media , most anaerobic bacteria are inhibited at Eh values higher than - 100 mV . Some will not initiate growth at potentials ...
Page 74
Reducing agents for anaerobic media along with other reducing agents below ) . E Compounds Concn in media ( mV ) 6.6.2 . Reducing Agents Sodium thioglycolate < -100 0.05 % Cysteine . HCI -210 ( 22 ) 0.025 % Reducing agents are added to ...
Reducing agents for anaerobic media along with other reducing agents below ) . E Compounds Concn in media ( mV ) 6.6.2 . Reducing Agents Sodium thioglycolate < -100 0.05 % Cysteine . HCI -210 ( 22 ) 0.025 % Reducing agents are added to ...
Page 509
... 418 ments , 87 Anaerobic chambers for stringent anaerobes , 76–77 Actinomyces bovis , media and cultural requirements , Anaerobic jars , 74-75 87 Anaerobiosis Actinomycetes and related organisms , key to media anaerobic chambers for ...
... 418 ments , 87 Anaerobic chambers for stringent anaerobes , 76–77 Actinomyces bovis , media and cultural requirements , Anaerobic jars , 74-75 87 Anaerobiosis Actinomycetes and related organisms , key to media anaerobic chambers for ...
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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