Manual of Methods for General Bacteriology |
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Page 68
10 , and if 1 pH unit below the pK , the ratio is When cultures are incubated in
atmospheres about 10 : 1 . For example , to prepare 100 ml of a enriched in CO2
, the carbonic acid - bicarbonate 0 . 1 M sodium phosphate buffer at pH 7 .
10 , and if 1 pH unit below the pK , the ratio is When cultures are incubated in
atmospheres about 10 : 1 . For example , to prepare 100 ml of a enriched in CO2
, the carbonic acid - bicarbonate 0 . 1 M sodium phosphate buffer at pH 7 .
Page 201
Philipp Gerhardt, American Society for Microbiology. 11 . 5 . 4 . RATIO
ACCURACY 201 Poisson error of a colony count and the error of Poisson
counting error . Imagine that each pipetthe dilution procedure both contribute to
the ting operation ...
Philipp Gerhardt, American Society for Microbiology. 11 . 5 . 4 . RATIO
ACCURACY 201 Poisson error of a colony count and the error of Poisson
counting error . Imagine that each pipetthe dilution procedure both contribute to
the ting operation ...
Page 456
Store the RNA in SSC containing 1 % A234 / A260 ratio is a rather sensitive
indicator of SDS at — 20°C or colder . contaminating material in a DNA
preparation . ( i ) The absorption maximum of phenol is 270 The total RNA , as
isolated above ...
Store the RNA in SSC containing 1 % A234 / A260 ratio is a rather sensitive
indicator of SDS at — 20°C or colder . contaminating material in a DNA
preparation . ( i ) The absorption maximum of phenol is 270 The total RNA , as
isolated above ...
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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