Manual of Methods for General Bacteriology |
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Page 17
Cover slip forceps . Forceps with flat , nonserrated gripping surfaces bent at an angle of 30 ° are convenient for picking up cover slips . Curved , pointed , and nonserrated jeweler's forceps are also ...
Cover slip forceps . Forceps with flat , nonserrated gripping surfaces bent at an angle of 30 ° are convenient for picking up cover slips . Curved , pointed , and nonserrated jeweler's forceps are also ...
Page 18
The the cells to the cover slip . The block may come higher concentrations are suitable for gram - posoff by itself . Separation may be assisted by holditive bacteria , while gram - negative bacteria may ing the cover slip down with ...
The the cells to the cover slip . The block may come higher concentrations are suitable for gram - posoff by itself . Separation may be assisted by holditive bacteria , while gram - negative bacteria may ing the cover slip down with ...
Page 23
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 does not colloidal particle causes the edge of the dark contact the ...
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 does not colloidal particle causes the edge of the dark contact the ...
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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