Manual of Methods for General Bacteriology |
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Page 120
17 ) and E broth ( 8 . 5 . 18 ) , dium such as TCBS agar ( 8 . 5 . 50 ) . Also
inoculate to select for mycoplasmas from the respiratory swabs of stool material
into an enrichment broth tract . Extract specimens collected on swabs into ( 1 %
peptone ...
17 ) and E broth ( 8 . 5 . 18 ) , dium such as TCBS agar ( 8 . 5 . 50 ) . Also
inoculate to select for mycoplasmas from the respiratory swabs of stool material
into an enrichment broth tract . Extract specimens collected on swabs into ( 1 %
peptone ...
Page 172
Filter aid may be added directly to the culture broth or prelayered on the filter
support . The practice of adding filter aid , such as cellulose , to the culture broth
can allow filtration of as much as 10 times the culture broth that can be treated by
...
Filter aid may be added directly to the culture broth or prelayered on the filter
support . The practice of adding filter aid , such as cellulose , to the culture broth
can allow filtration of as much as 10 times the culture broth that can be treated by
...
Page 411
In the case of anaerobes cultured in prereduced PY broth ( 20 . 3 . 28 ) containing
carbohydrates , the oxygen - free carbon dioxide used to purge the tube during
their inoculation will usually lower the pH of the medium to 6 . 2 to 6 . 4 .
In the case of anaerobes cultured in prereduced PY broth ( 20 . 3 . 28 ) containing
carbohydrates , the oxygen - free carbon dioxide used to purge the tube during
their inoculation will usually lower the pH of the medium to 6 . 2 to 6 . 4 .
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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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Common terms and phrases
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