Manual of Methods for General Bacteriology |
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Page 18
The cover slip , with undisturbed culture and medium attached , must be removed
from the slide for appropriate fixation and embedding in plastic . This can be
facilitated by fashioning a " handle " of a strip of Mylar tape or a self - stick label to
...
The cover slip , with undisturbed culture and medium attached , must be removed
from the slide for appropriate fixation and embedding in plastic . This can be
facilitated by fashioning a " handle " of a strip of Mylar tape or a self - stick label to
...
Page 19
3 . LITERATURE CITED 19 is very satisfactory . A similar coating of polyly . sine ,
which provides a positively charged interface , should be as effective or more so (
4 ) . 2 . Wash the cover slip in water . 3 . Stain it with Giemsa solution ( 10 drops ...
3 . LITERATURE CITED 19 is very satisfactory . A similar coating of polyly . sine ,
which provides a positively charged interface , should be as effective or more so (
4 ) . 2 . Wash the cover slip in water . 3 . Stain it with Giemsa solution ( 10 drops ...
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 bottom of the well ...
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 bottom of the well ...
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Contents
55 | 32 |
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 acids amount anaerobic applications appropriate assay autoclaving bacteria Bacteriol base broth buffer cells centrifuge colonies column components compounds concentration containing counting cover culture described determine dilution Dissolve distilled water effective electron enrichment enzyme examine example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter microscopy mixture mutants obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts sample selection separation slide sodium solution specific staining standard sterile substrate surface suspension Table techniques temperature tion transfer tube usually values vitamin volume Wash York