Manual of Methods for General Bacteriology |
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Res . 26 : 31-43 . 54. Glauert , A. M. , M. J. Thornley , K. J. I. Thorne , and U. B. Sleytr . 1976. In R. Fuller and D. W. Lovelock ( ed . ) , Microbial ultrastructure . The use of the electron microscope , p . 31-47 . Academic Press ...
Res . 26 : 31-43 . 54. Glauert , A. M. , M. J. Thornley , K. J. I. Thorne , and U. B. Sleytr . 1976. In R. Fuller and D. W. Lovelock ( ed . ) , Microbial ultrastructure . The use of the electron microscope , p . 31-47 . Academic Press ...
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Cambridge Press , Cambridge . Excellent , critical discussion of techniques and methods . 6. Miller , J. H. 1972. Experiments in molecular genetics . Cold Spring Harbor Laboratory , Cold Spring Harbor , N.Y. 7. Pirt , S. J. 1975.
Cambridge Press , Cambridge . Excellent , critical discussion of techniques and methods . 6. Miller , J. H. 1972. Experiments in molecular genetics . Cold Spring Harbor Laboratory , Cold Spring Harbor , N.Y. 7. Pirt , S. J. 1975.
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Academic Press , Inc. , New York . 3. Bender , R. A. , K. A. Janssen , A. D. Resnick , M. Blumberg , F. Foor , and B. Magasanik . 1977. J. Bacteriol . 129 : 1001-1009 . 4. Buttin , G. 1963. J. Mol . Biol . 7 : 164-182 . 5.
Academic Press , Inc. , New York . 3. Bender , R. A. , K. A. Janssen , A. D. Resnick , M. Blumberg , F. Foor , and B. Magasanik . 1977. J. Bacteriol . 129 : 1001-1009 . 4. Buttin , G. 1963. J. Mol . Biol . 7 : 164-182 . 5.
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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