Manual of Methods for General Bacteriology |
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Page 368
Most of the other techniques have ally hydrolases such as alkaline phosphatase , specialized uses or are effective only with orgaribonuclease I , and cyclic phosphodiesterase . nisms ( such as protozoans or animal tissues ) The method ...
Most of the other techniques have ally hydrolases such as alkaline phosphatase , specialized uses or are effective only with orgaribonuclease I , and cyclic phosphodiesterase . nisms ( such as protozoans or animal tissues ) The method ...
Page 369
This , comNossal ( McDonald Engineering Co. , Bay Village , bined with its effectiveness in breaking a wide Ohio ) ... A much more effective techsound is caused by cavitational forces producing nique for solid shear disruption of bacteria ...
This , comNossal ( McDonald Engineering Co. , Bay Village , bined with its effectiveness in breaking a wide Ohio ) ... A much more effective techsound is caused by cavitational forces producing nique for solid shear disruption of bacteria ...
Page 500
Clean surfaces or clear water can be effectively treated by 75 ppm of available iodine , but difficulties may be ... An alcoholic solution ( tincture ) of iodine is effective as a disinfectant , but is irritating Heavy metals are not ...
Clean surfaces or clear water can be effectively treated by 75 ppm of available iodine , but difficulties may be ... An alcoholic solution ( tincture ) of iodine is effective as a disinfectant , but is irritating Heavy metals are not ...
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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