Manual of Methods for General Bacteriology |
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Page 292
Photochemical decomposition and adsorption to glass surfaces , especially for
macromolecules , are quite common . The former can be detected as a loss of
fluorescence with time , and the latter can be suspected if there is an apparent
lag in ...
Photochemical decomposition and adsorption to glass surfaces , especially for
macromolecules , are quite common . The former can be detected as a loss of
fluorescence with time , and the latter can be suspected if there is an apparent
lag in ...
Page 340
Glass chromatographic tube approximately 1 by 30 cm , fitted with a solvent
reservoir ( separatory funnel with a Teflon stopcock ) coupled to the top of the
column by a 24 / 49 or standard taper greaseless glass joint . The column should
be ...
Glass chromatographic tube approximately 1 by 30 cm , fitted with a solvent
reservoir ( separatory funnel with a Teflon stopcock ) coupled to the top of the
column by a 24 / 49 or standard taper greaseless glass joint . The column should
be ...
Page 341
Acid - washed glass beads and marbles : Clean with the test tubes above .
Perchloric acid ( 72 % , vol / vol ) in distilled water ( CAUTION : Perchloric acid
liquid and vapors cause burns . Wear protective gloves , clothing , and goggles .
Acid - washed glass beads and marbles : Clean with the test tubes above .
Perchloric acid ( 72 % , vol / vol ) in distilled water ( CAUTION : Perchloric acid
liquid and vapors cause burns . Wear protective gloves , clothing , and goggles .
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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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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