Manual of Methods for General Bacteriology |
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Page 68
Philipp Gerhardt, American Society for Microbiology. of acidic solution to basic
solution is about 1 : 1 ; if 1 pH unit above the pK , the ratio is about 1 : 10 ; and if 1
pH unit below the pK , the ratio is about 10 : 1 . For example , to prepare 100 ml of
...
Philipp Gerhardt, American Society for Microbiology. of acidic solution to basic
solution is about 1 : 1 ; if 1 pH unit above the pK , the ratio is about 1 : 10 ; and if 1
pH unit below the pK , the ratio is about 10 : 1 . For example , to prepare 100 ml of
...
Page 201
RATIO ACCURACY 201 Poisson error of a colony count and the error of the
dilution procedure both contribute to the error in the estimated concentration of
organisms of the original undiluted suspension . Generally , additional errors can
only ...
RATIO ACCURACY 201 Poisson error of a colony count and the error of the
dilution procedure both contribute to the error in the estimated concentration of
organisms of the original undiluted suspension . Generally , additional errors can
only ...
Page 317
Long counts are not needed at low radioactivity levels as for the channel ratio
method . It is possible to improve the external standard method described above
by making a channel ratio approach with and without the gamma source .
Long counts are not needed at low radioactivity levels as for the channel ratio
method . It is possible to improve the external standard method described above
by making a channel ratio approach with and without the gamma source .
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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