Manual of Methods for General Bacteriology |
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Page 351
Colored samples Particulates Ions of Sb Bi Fe ( III ) Pb Hg Ag Cu ( III ) Auric
Chloroplatinate Metavanadate Reduction to NH4 + by hot > 2 mg / liter NO3 - ,
NH4 + Good when [ NO2 ] > 2 , 000 Hot alkali , requires distilalkali or salicylic
acid ug ...
Colored samples Particulates Ions of Sb Bi Fe ( III ) Pb Hg Ag Cu ( III ) Auric
Chloroplatinate Metavanadate Reduction to NH4 + by hot > 2 mg / liter NO3 - ,
NH4 + Good when [ NO2 ] > 2 , 000 Hot alkali , requires distilalkali or salicylic
acid ug ...
Page 355
The pres - ence of any of these may indicate the use of an alternate method of
NO2 detection , such as reduction and subsequent analysis as NH4 + . AS with
any colorimetric procedure , colored or par - ticulate substances in the sample
may ...
The pres - ence of any of these may indicate the use of an alternate method of
NO2 detection , such as reduction and subsequent analysis as NH4 + . AS with
any colorimetric procedure , colored or par - ticulate substances in the sample
may ...
Page 356
After either of the reduction procedures de column with dilute NH4Cl solution or
with the scribed here , the analysis for NO2 is performed supernatant fraction
from the Cd - Cu amalgaas outlined above in the method for nitrite . Since mation
...
After either of the reduction procedures de column with dilute NH4Cl solution or
with the scribed here , the analysis for NO2 is performed supernatant fraction
from the Cd - Cu amalgaas outlined above in the method for nitrite . Since mation
...
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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