Manual of Methods for General Bacteriology |
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Page 108
J . Bacteriol . 115 : 367 - 386 . 37 . Couch , J . N . 1950 . J . Elisha Mitchell Sci .
Soc . 66 : 87 – 92 . 38 . Couch , J . N . 1955 ... J . Elisha Mitchell Sci . Soc . 79 : 53
– 70 . 40 . Craig , J . A . , and E . E . Snell . 1951 . J . Bacteriol . 61 : 283 – 291 . 41
.
J . Bacteriol . 115 : 367 - 386 . 37 . Couch , J . N . 1950 . J . Elisha Mitchell Sci .
Soc . 66 : 87 – 92 . 38 . Couch , J . N . 1955 ... J . Elisha Mitchell Sci . Soc . 79 : 53
– 70 . 40 . Craig , J . A . , and E . E . Snell . 1951 . J . Bacteriol . 61 : 283 – 291 . 41
.
Page 110
J . Bacteriol . 97 : 561 - 570 . 148 . Moss , C . W . , V . R . Dowell , Jr . , V . J . Lewis
, and M . A . Schekter . 1967 . J . Bacteriol . 94 : 1300 - 1305 . 149 . Mueller , J . H .
1938 . J . Bacteriol . 36 : 499 - 515 . 150 . Mulder , E . G . 1964 . J . Appl ...
J . Bacteriol . 97 : 561 - 570 . 148 . Moss , C . W . , V . R . Dowell , Jr . , V . J . Lewis
, and M . A . Schekter . 1967 . J . Bacteriol . 94 : 1300 - 1305 . 149 . Mueller , J . H .
1938 . J . Bacteriol . 36 : 499 - 515 . 150 . Mulder , E . G . 1964 . J . Appl ...
Page 111
4 LITERATURE CITED 111 Bacteriol . 127 : 780 – 784 . 208 . Stadtman , E . R . ,
T . C . Stadtman , I . Pastan , and L . DS . Smith . 1972 . J . Bacteriol . 110 : 758 -
760 . 209 . Stadtman , T . C . , and H . A . Barker . 1951 . J . Bacteriol . 61 : 67 – 80
.
4 LITERATURE CITED 111 Bacteriol . 127 : 780 – 784 . 208 . Stadtman , E . R . ,
T . C . Stadtman , I . Pastan , and L . DS . Smith . 1972 . J . Bacteriol . 110 : 758 -
760 . 209 . Stadtman , T . C . , and H . A . Barker . 1951 . J . Bacteriol . 61 : 67 – 80
.
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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