Manual of Methods for General Bacteriology: By Philipp Gerhardt, Editor-in-chief ; R.G.E. Murray, Editor, I. Morphology ... [et Al.].Philipp Gerhardt, American Society for Microbiology |
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Page 308
critical applications requires, as it does for all other chromatographic separations,
properly designed columns and associated equipment. Attention is called to the
fact that “mixing reservoirs" above and below the gel bed must be avoided; ...
critical applications requires, as it does for all other chromatographic separations,
properly designed columns and associated equipment. Attention is called to the
fact that “mixing reservoirs" above and below the gel bed must be avoided; ...
Page 356
Preparation of columns. Columns should be 1 by 30 cm with an appropriate
opening (e.g., thistle tube or funnel) at the top so that the total sample can be
placed on the column at once. The bottom of the column should have a burette-
type ...
Preparation of columns. Columns should be 1 by 30 cm with an appropriate
opening (e.g., thistle tube or funnel) at the top so that the total sample can be
placed on the column at once. The bottom of the column should have a burette-
type ...
Page 424
Use a column 6 ft (1.8 m) long and 0.25 in. (6 mm) in diameter, of stainless steel,
aluminum, or glass. Pack the column with Supelco SP-1000, 100 to 200 mesh (
Supelco Inc., Bellefonte, Pa.), or with 5% FFAP on Chromosorb-G. Both volatile ...
Use a column 6 ft (1.8 m) long and 0.25 in. (6 mm) in diameter, of stainless steel,
aluminum, or glass. Pack the column with Supelco SP-1000, 100 to 200 mesh (
Supelco Inc., Bellefonte, Pa.), or with 5% FFAP on Chromosorb-G. Both volatile ...
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Contents
MORPHOLOGY | 5 |
Light Microscopy R G E MURRAY AND C F Robinow 2 Specimen Preparation for Light Microscopy R G E MURRAY AND C F Robi | 17 |
Determinative Methods of Light Microscopy R N DoETscH | 21 |
Copyright | |
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acetate Adjust agar allow amino acids anaerobic aqueous assay autoclaving bacteria bacterial cells Bacteriol bacteriology bacterium biotin broth buffer carbon centrifuge chemical coli colonies column components compounds concentration containing cover slip culture described detergents determined dilution Dissolve distilled water electron microscopy endospores enzyme Escherichia coli ethanol film filter final first flask fraction g Distilled genetic glass glucose gradient gram-negative gram-positive grid growth heat hydroxylapatite Incubate inoculated isolation laboratory lipids liquid liter measure medium membrane metabolic method mg/liter Microbiol microbiology mixture mutagens mutants NaCl nitrogen nutrient organisms oxidation oxygen Pasteur pipette pellet phage pipette plasmid plate prepared procedure protein radioactivity reaction reagent remove sample slide sodium solution specific spheroplasts staining standard sterile substrate sucrose surface suspension Table techniques temperature thiamine tion tube vials vitamin vol/vol volume Wash wt/vol yeast extract