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
Bubble interference can be eliminated by using an Sampling procedure . external flow - through optical cell ; however , Sampling is best accomplished with an inde- foaming continues to be a problem . Wall growth pendent sample line ...
Bubble interference can be eliminated by using an Sampling procedure . external flow - through optical cell ; however , Sampling is best accomplished with an inde- foaming continues to be a problem . Wall growth pendent sample line ...
Page 357
Samples . Samples should be treated as described in part 17.6.1 . Samples high in interfering compounds ( see Table 1 ) ... Prepare fresh for each sample group , as NH , * fumes from the laboratory will rapidly contaminate the water .
Samples . Samples should be treated as described in part 17.6.1 . Samples high in interfering compounds ( see Table 1 ) ... Prepare fresh for each sample group , as NH , * fumes from the laboratory will rapidly contaminate the water .
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Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
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Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York