Manual of Methods for General Bacteriology |
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Page 200
1 ml of these dilutions were plated , then 2 . 2 x 10 - 6 ml was the total volume of
original culture used to make the four plates . Therefore , the best estimate of the
concentration is 1 , 206 / 2 . 2 x 107° = 5 . 46 x 10° / ml . The standard deviation is
...
1 ml of these dilutions were plated , then 2 . 2 x 10 - 6 ml was the total volume of
original culture used to make the four plates . Therefore , the best estimate of the
concentration is 1 , 206 / 2 . 2 x 107° = 5 . 46 x 10° / ml . The standard deviation is
...
Page 291
Standard statistical considerations apply , i . e . , replication , least - square fits of
the data to straight lines , determination of standard devia - tion from the mean ,
and standard error . Although linearity is highly desired , it is also pos - sible to ...
Standard statistical considerations apply , i . e . , replication , least - square fits of
the data to straight lines , determination of standard devia - tion from the mean ,
and standard error . Although linearity is highly desired , it is also pos - sible to ...
Page 358
After 30 min or tionally smaller volumes of sample , standards , longer at room
temperature , measure the aband reagents ... Calculate the amount of ammonia
in appropriate spectrophotometer is available . each sample from a standard
curve ...
After 30 min or tionally smaller volumes of sample , standards , longer at room
temperature , measure the aband reagents ... Calculate the amount of ammonia
in appropriate spectrophotometer is available . each sample from a standard
curve ...
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Contents
55 | 32 |
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 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 enrichment enzyme examine 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 microscopy mixture mutants 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