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 315
Once this has been determined, the lower discriminator is set to exclude most of
the background (i.e., set at 10) and the upper is set to just include the maximum
pulse height of the isotope being measured. In this way much of the low-energy ...
Once this has been determined, the lower discriminator is set to exclude most of
the background (i.e., set at 10) and the upper is set to just include the maximum
pulse height of the isotope being measured. In this way much of the low-energy ...
Page 361
The retention times for acetylene and ethylene are determined by the gas
chromatograph set-up as specified by the manufacturer or supplier of the packing
material, or can be determined by using acetylene and ethylene standards.
The retention times for acetylene and ethylene are determined by the gas
chromatograph set-up as specified by the manufacturer or supplier of the packing
material, or can be determined by using acetylene and ethylene standards.
Page 389
Samples are then removed and the radioactivity is determined (with appropriate
quench corrections made) in a liquid scintillation counter (16.4.3). In this way an
accounting of the total "CO2 resulting from the metabolism of the labeled glucose
...
Samples are then removed and the radioactivity is determined (with appropriate
quench corrections made) in a liquid scintillation counter (16.4.3). In this way an
accounting of the total "CO2 resulting from the metabolism of the labeled glucose
...
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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