Manual of Methods for General Bacteriology |
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Page 54
Neither of these devices had any provision The major disadvantage is that
breakage is for cooling the sample during shaking , and it was not instantaneous
, and a cell suspension must be necessary to interrupt the shaking frequently to ...
Neither of these devices had any provision The major disadvantage is that
breakage is for cooling the sample during shaking , and it was not instantaneous
, and a cell suspension must be necessary to interrupt the shaking frequently to ...
Page 165
Follow the fermentor manufacturer ' s instruction for sampling during continuous
cultivation . If an external sampling system is used in place of sample collection
from the effluent line , the sam ple size must be kept below 10 % of the reactor ...
Follow the fermentor manufacturer ' s instruction for sampling during continuous
cultivation . If an external sampling system is used in place of sample collection
from the effluent line , the sam ple size must be kept below 10 % of the reactor ...
Page 356
Since mation ; then slowly pour in the Cd - Cu filings the analysis is for total NO2 ,
part of the sample and let them settle until a ... Add 2 ml of concentrated NH4Cl
Samples should be treated as described above reagent to 100 ml of the sample .
Since mation ; then slowly pour in the Cd - Cu filings the analysis is for total NO2 ,
part of the sample and let them settle until a ... Add 2 ml of concentrated NH4Cl
Samples should be treated as described above reagent to 100 ml of the sample .
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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