Manual of Methods for General Bacteriology |
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Page 26
Solution B for staining reagent : Ammonium oxalate , 0.8 g Distilled water , 80 ml Mix A and B to obtain the crystal violet staining reagent . Store for 24 h and filter through paper before using Mordant : Iodine , 1.0 g Potassium ...
Solution B for staining reagent : Ammonium oxalate , 0.8 g Distilled water , 80 ml Mix A and B to obtain the crystal violet staining reagent . Store for 24 h and filter through paper before using Mordant : Iodine , 1.0 g Potassium ...
Page 40
A whether or not a bacterium is gram positive . satisfactory grid prepared by the drop with- Negative staining also is a convenient means drawal method will show a gradient of particle of following the course of cell disruption or of ...
A whether or not a bacterium is gram positive . satisfactory grid prepared by the drop with- Negative staining also is a convenient means drawal method will show a gradient of particle of following the course of cell disruption or of ...
Page 322
containing 1 ug of protein is normally visible after staining with Coomassie blue . Care must be taken that some of the sample is not lost to the electrode solution . a Analysis of gels . Direct scanning . For both proteins and nucleic ...
containing 1 ug of protein is normally visible after staining with Coomassie blue . Care must be taken that some of the sample is not lost to the electrode solution . a Analysis of gels . Direct scanning . For both proteins and nucleic ...
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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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Common terms and phrases
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