Manual of Methods for General Bacteriology |
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Page 23
a sion slide in such a manner that the drop does negatively charged . When films of these colloids not run down the cover slip . The drop of sample dry , the similar charge on both bacterium and must be sufficiently small so that it ...
a sion slide in such a manner that the drop does negatively charged . When films of these colloids not run down the cover slip . The drop of sample dry , the similar charge on both bacterium and must be sufficiently small so that it ...
Page 30
+ S a by heating loosely packed slides at 400 ° C for 20 ( wt / vol ) Sudan black B made up in ethylene min in a muffle ... Drain , and air dry the slide on blotting allowed to dry on slides in a thin film and paper . removed with a ...
+ S a by heating loosely packed slides at 400 ° C for 20 ( wt / vol ) Sudan black B made up in ethylene min in a muffle ... Drain , and air dry the slide on blotting allowed to dry on slides in a thin film and paper . removed with a ...
Page 430
Rock the slide in a circular fashion for 1 min to further mix the cells and liquid , being careful not to spill over the boundary of the ring . Examine the slide by eye ; for best visibility hold the slide near a bright light and view ...
Rock the slide in a circular fashion for 1 min to further mix the cells and liquid , being careful not to spill over the boundary of the ring . Examine the slide by eye ; for best visibility hold the slide near a bright light and view ...
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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