Manual of Methods for General Bacteriology |
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Page 54
Neither of these devices had any provision The major disadvantage is that
breakage is for cooling the sample during shaking , and it was not instantaneous
, and a cell suspension must be necessary to interrupt the shaking frequently to ...
Neither of these devices had any provision The major disadvantage is that
breakage is for cooling the sample during shaking , and it was not instantaneous
, and a cell suspension must be necessary to interrupt the shaking frequently to ...
Page 59
Bromophenol blue or phenol red and because the gels may be rapidly fixed after
can also be added to the sample to serve as a electrophoresis to minimize
diffusion of protein tracking dye . The final samples should contain bands .
Bromophenol blue or phenol red and because the gels may be rapidly fixed after
can also be added to the sample to serve as a electrophoresis to minimize
diffusion of protein tracking dye . The final samples should contain bands .
Page 357
357 Samples . Samples should be treated as described in part 17 . 6 . 1 .
Samples high in interfering compounds ( see Table 1 ) ... Prepare fresh for each
sample group , as NH * fumes from the laboratory will rapidly contaminate the
water .
357 Samples . Samples should be treated as described in part 17 . 6 . 1 .
Samples high in interfering compounds ( see Table 1 ) ... Prepare fresh for each
sample group , as NH * fumes from the laboratory will rapidly contaminate the
water .
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
Copyright | |
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Common terms and phrases
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 enzyme 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 Microbiol microscopy mixture mutants needed 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
Bibliographic information
| Title | Manual of Methods for General Bacteriology |
| Author | Philipp Gerhardt |
| Editor | Philipp Gerhardt |
| Contributors | R. G. E. Murray, Ralph N. Costilow, American Society for Microbiology, Willis A. Wood |
| Edition | illustrated, reprint |
| Publisher | American Society for Microbiology, 1981 |
| Original from | the University of Michigan |
| Digitized | 17 Jul 2008 |
| ISBN | 0914826298, 9780914826293 |
| Length | 524 pages |
| Export Citation | BiBTeX EndNote RefMan |