Manual of Methods for General Bacteriology |
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Page 300
If the other proteins are eluted preferentially , the adsorbent should be treated with eluant with increasing ionic strength with or without pH change until significant amounts of desired material appear in the eluate .
If the other proteins are eluted preferentially , the adsorbent should be treated with eluant with increasing ionic strength with or without pH change until significant amounts of desired material appear in the eluate .
Page 347
Half Good examples of approaches for a more com- the suspended organic material in the supernaplete characterization of ... Lipopolysaccharides ( 42 ) the sediment five times to wash it free from Reagents , materials , and equipment ...
Half Good examples of approaches for a more com- the suspended organic material in the supernaplete characterization of ... Lipopolysaccharides ( 42 ) the sediment five times to wash it free from Reagents , materials , and equipment ...
Page 492
Take care not to contaminate the When recovering the contents of an ampoule , culture material with the disinfectant . Also , if take care not to cut the gloves or hands or to the tube breaks , the disinfectant may not comdisperse ...
Take care not to contaminate the When recovering the contents of an ampoule , culture material with the disinfectant . Also , if take care not to cut the gloves or hands or to the tube breaks , the disinfectant may not comdisperse ...
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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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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