Manual of Methods for General Bacteriology |
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Page 308
critical applications requires , as it does for all other chromatographic separations
, properly de - signed columns and associated equipment . ... Column length
affects resolution and column cross - sectional area is proportional to capacity .
critical applications requires , as it does for all other chromatographic separations
, properly de - signed columns and associated equipment . ... Column length
affects resolution and column cross - sectional area is proportional to capacity .
Page 340
When this solvent mixture just enters the resin bed , add 60 ml of acetone and
collect in the same vessel ; then add 60 ml of methanol to the column and collect
the eluate in the third vessel . The first collection vessel will contain neutral lipids
...
When this solvent mixture just enters the resin bed , add 60 ml of acetone and
collect in the same vessel ; then add 60 ml of methanol to the column and collect
the eluate in the third vessel . The first collection vessel will contain neutral lipids
...
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