Manual of Methods for General Bacteriology |
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Page 288
Philipp Gerhardt, American Society for Microbiology. K N ATURAL BAND WIDTH
- Absorbance ( A ) ; Intensity ( B ) SPECTRAL BAND WIDTH 270 290 310 330
350 370 390 Wave length ( nm ) Fig . 1 . ( A ) Natural bandwidth diagram of
NADH ...
Philipp Gerhardt, American Society for Microbiology. K N ATURAL BAND WIDTH
- Absorbance ( A ) ; Intensity ( B ) SPECTRAL BAND WIDTH 270 290 310 330
350 370 390 Wave length ( nm ) Fig . 1 . ( A ) Natural bandwidth diagram of
NADH ...
Page 289
0 O True absorbance True absorbance Fig . 3 . ( A ) Plot of measured ( Ao )
versus true ( Ar ) absorbance for a spectrophotometer . ( B ) Plot of absorbance
error ( AA / AAT ) versus true absorbance . the use of pure reagents . In addition ,
errors.
0 O True absorbance True absorbance Fig . 3 . ( A ) Plot of measured ( Ao )
versus true ( Ar ) absorbance for a spectrophotometer . ( B ) Plot of absorbance
error ( AA / AAT ) versus true absorbance . the use of pure reagents . In addition ,
errors.
Page 456
Repeat the ethanol precipitation , centrif - acid preparation and contributes to a
large peak ugation , and dissolution until the supernatant at 208 nm , the peak
will overlap the 234 - nm after centrifuging has a negligible absorbance at
minimum ...
Repeat the ethanol precipitation , centrif - acid preparation and contributes to a
large peak ugation , and dissolution until the supernatant at 208 nm , the peak
will overlap the 234 - nm after centrifuging has a negligible absorbance at
minimum ...
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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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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