Manual of Methods for General Bacteriology |
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Page 30
Rinse the slide with tap water , blot dry , and examine . Poly - ß - hydroxybutyrate
inclusions appear as blue - black droplets , and cytoplasmic parts of the organism
appear pink . Leifson method for staining flagella . Solution 1 : Sodium chloride ...
Rinse the slide with tap water , blot dry , and examine . Poly - ß - hydroxybutyrate
inclusions appear as blue - black droplets , and cytoplasmic parts of the organism
appear pink . Leifson method for staining flagella . Solution 1 : Sodium chloride ...
Page 31
Wash the slide in tap water , blot dry , and examine . Procedure : Polysaccharides
stain red , and other cytoplas1 . Using slides cleaned in the manner demic
components are green . scribed for making suitable flagellar stains , air dry a film
of ...
Wash the slide in tap water , blot dry , and examine . Procedure : Polysaccharides
stain red , and other cytoplas1 . Using slides cleaned in the manner demic
components are green . scribed for making suitable flagellar stains , air dry a film
of ...
Page 414
bate at 37°C and examine at 4 and 24 h . Positive test : solid clot or a loose clot
suspended in the plasma . Granular or ropy formations are incon - clusive .
Examples : positive , Staphylococcus aureus ; negative , Staphylococcus
epidermidis ...
bate at 37°C and examine at 4 and 24 h . Positive test : solid clot or a loose clot
suspended in the plasma . Granular or ropy formations are incon - clusive .
Examples : positive , Staphylococcus aureus ; negative , Staphylococcus
epidermidis ...
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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