Manual of Methods for General Bacteriology |
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Page 125
Prepare a 1 : 10 dilution of soil . and inoculate each flask of the enrichment me
dium with 1 . 0 ml of the dilution . Incubate at 28°C . At weekly intervals , test for
disappearance of the ammonium or nitrite by removing samples of the
enrichment ...
Prepare a 1 : 10 dilution of soil . and inoculate each flask of the enrichment me
dium with 1 . 0 ml of the dilution . Incubate at 28°C . At weekly intervals , test for
disappearance of the ammonium or nitrite by removing samples of the
enrichment ...
Page 513
... 85 Desulfotomaculum , enrichment and isolation , 125 - 126 Desulfotomaculum
acetoxidans , enrichment and isolation ... 504 Dilute media , use in enrichment
techniques , 122 – 123 Diphenylamine assay for DNA , 456 - 457 Diphenylamine
...
... 85 Desulfotomaculum , enrichment and isolation , 125 - 126 Desulfotomaculum
acetoxidans , enrichment and isolation ... 504 Dilute media , use in enrichment
techniques , 122 – 123 Diphenylamine assay for DNA , 456 - 457 Diphenylamine
...
Page 521
SUBJECT INDEX 521 Pseudomonas maltophilia , media and cultural
requirements , 86 Pseudomonas putida enrichment and isolation , 125 lipase ,
418 media and cultural requirements , 86 Pseudomonas testosteroni , media and
cultural ...
SUBJECT INDEX 521 Pseudomonas maltophilia , media and cultural
requirements , 86 Pseudomonas putida enrichment and isolation , 125 lipase ,
418 media and cultural requirements , 86 Pseudomonas testosteroni , media and
cultural ...
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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