Manual of Methods for General Bacteriology |
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Page 200
The standard deviation is as indicated above . V1,206 / 2.2 x 10-6 = +0.16 x 108 /
ml . Justification for treating the results at the two 11.5.2 Statistical Tests different
dilutions separately and not pooling Much of the statistics taught in elementary ...
The standard deviation is as indicated above . V1,206 / 2.2 x 10-6 = +0.16 x 108 /
ml . Justification for treating the results at the two 11.5.2 Statistical Tests different
dilutions separately and not pooling Much of the statistics taught in elementary ...
Page 317
Since quenching may be due to colorless chemicals such as water and CCL ,
and also to colored compounds , it may be difficult to prepare standards of the
same quencher content as the unknowns . Thus , there will be some error if
colored ...
Since quenching may be due to colorless chemicals such as water and CCL ,
and also to colored compounds , it may be difficult to prepare standards of the
same quencher content as the unknowns . Thus , there will be some error if
colored ...
Page 358
After 30 min or tionally smaller volumes of sample , standards , longer at room
temperature , measure the aband reagents ... Calculate the amount of ammonia
in appropriate spectrophotometer is available . each sample from a standard
curve ...
After 30 min or tionally smaller volumes of sample , standards , longer at room
temperature , measure the aband reagents ... Calculate the amount of ammonia
in appropriate spectrophotometer is available . each sample from a standard
curve ...
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Contents
MORPHOLOGY | 5 |
NOW | 17 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
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 examine example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plate positive prepared present Press procedure protein reaction reagent references remove 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