Manual of Methods for General Bacteriology |
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Page 41
Allow to stand , with 4. Suspend the washed pellet in 1 % osmium occasional mixing , for 30 min or until cubes sink tetroxide for 6 to 16 h at room temperature . to the bottom of the vial . ( The medium is most ( The glutaraldehyde ...
Allow to stand , with 4. Suspend the washed pellet in 1 % osmium occasional mixing , for 30 min or until cubes sink tetroxide for 6 to 16 h at room temperature . to the bottom of the vial . ( The medium is most ( The glutaraldehyde ...
Page 128
Flame - sterilize the loop and allow it to However , one often needs to dilute the sample cool ( 15 s ) . ( C ) Draw the loop over section 1 as shown , in order to obtain well - isolated colonies , and the and immediately streak back ...
Flame - sterilize the loop and allow it to However , one often needs to dilute the sample cool ( 15 s ) . ( C ) Draw the loop over section 1 as shown , in order to obtain well - isolated colonies , and the and immediately streak back ...
Page 166
The pH meter and pH titrator must be interconnected and therefore should probably be purchased from the same manufacturer to ensure equipment match . Although a peristaltic pump can allow foolproof addition of acid or base against ...
The pH meter and pH titrator must be interconnected and therefore should probably be purchased from the same manufacturer to ensure equipment match . Although a peristaltic pump can allow foolproof addition of acid or base against ...
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Contents
1 | 22 |
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 amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York