Manual of Methods for General Bacteriology |
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Page 29
Procedure : Immerse the specimen in the reagent and examine the wet
preparation . Vegetative azoto - bacters are yellowish green ; early encystment
stages appear with a darker green cytoplasm somewhat receded from the outer
cell wall ...
Procedure : Immerse the specimen in the reagent and examine the wet
preparation . Vegetative azoto - bacters are yellowish green ; early encystment
stages appear with a darker green cytoplasm somewhat receded from the outer
cell wall ...
Page 30
Rinse the slide with tap water , blot dry , and examine . Leifson method for
staining flagella . Poly - B - hydroxybutyrate inclusions appear as Solution 1 :
blue - black droplets , and cytoplasmic parts of the Sodium chloride , 1 . 5 g
organism ...
Rinse the slide with tap water , blot dry , and examine . Leifson method for
staining flagella . Poly - B - hydroxybutyrate inclusions appear as Solution 1 :
blue - black droplets , and cytoplasmic parts of the Sodium chloride , 1 . 5 g
organism ...
Page 31
Wash the slide in tap water , blot dry , and examine . Procedure : 1 . Using slides
cleaned in the manner dePolysaccharides stain red , and other cytoplasmic
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 : 1 . Using slides
cleaned in the manner dePolysaccharides stain red , and other cytoplasmic
components are green . scribed for making suitable flagellar stains , air dry a film
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