Manual of Methods for General Bacteriology |
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Page 119
For a clear , detailed exposition of the many intricacies of such enrichment and
the subsequent isolation of ... Subject a portion of this culture to sonic oscillation ,
and then use the pour - plate method to obtain isolated colonies as described in ...
For a clear , detailed exposition of the many intricacies of such enrichment and
the subsequent isolation of ... Subject a portion of this culture to sonic oscillation ,
and then use the pour - plate method to obtain isolated colonies as described in ...
Page 124
Prepare a secondary enrichment cul ture ; then purify by obtaining isolated
colonies on nitrogen - free agar medium ( Azotobacter me - dium ... For isolation
of cytophagas that are not obligate cellulose decomposers , streak onto tryptone
agar .
Prepare a secondary enrichment cul ture ; then purify by obtaining isolated
colonies on nitrogen - free agar medium ( Azotobacter me - dium ... For isolation
of cytophagas that are not obligate cellulose decomposers , streak onto tryptone
agar .
Page 142
Isolation of Gallionella ferruginea by use of formalin . Can . ... Isolation ,
cultivation and maintenance of the myxobacteria , p . ... Vibrio fetus var .
intestinalis isolated from fecal and intestinal contents of clinically normal sheep :
isolation of ...
Isolation of Gallionella ferruginea by use of formalin . Can . ... Isolation ,
cultivation and maintenance of the myxobacteria , p . ... Vibrio fetus var .
intestinalis isolated from fecal and intestinal contents of clinically normal sheep :
isolation of ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
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 enzyme 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 Microbiol microscopy mixture mutants needed 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