Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 81
Page 76
Transfer can also be made transfer . with stainless - steel or platinum loops . The V.P.I. 2. Fill the pipette used for transferring me- Anaerobic Culture System ( Bellco Glass , Inc. ) is dium with the gas prior to drawing medium into ...
Transfer can also be made transfer . with stainless - steel or platinum loops . The V.P.I. 2. Fill the pipette used for transferring me- Anaerobic Culture System ( Bellco Glass , Inc. ) is dium with the gas prior to drawing medium into ...
Page 243
Chapter 14 Gene Transfer ROY CURTISS III 14.1 . TRANSFORMATION 243 14.1.1 . Isolation of DNA 244 .2 . Quantitation of DNA 244 .3 . Transformation in Acinetobacter calcoaceticus 245 .4 . Transformation in Escherichia coli 247 14.2 .
Chapter 14 Gene Transfer ROY CURTISS III 14.1 . TRANSFORMATION 243 14.1.1 . Isolation of DNA 244 .2 . Quantitation of DNA 244 .3 . Transformation in Acinetobacter calcoaceticus 245 .4 . Transformation in Escherichia coli 247 14.2 .
Page 258
The donor harboring R100 drd - 1 optimal transfer frequencies when matings are should be sensitive to nalidixic acid and the conducted at or near 37 ° C . With some of these , recipient , such as strain 10 ( Table 1 ) , should not ...
The donor harboring R100 drd - 1 optimal transfer frequencies when matings are should be sensitive to nalidixic acid and the conducted at or near 37 ° C . With some of these , recipient , such as strain 10 ( Table 1 ) , should not ...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
7 other sections not shown
Other editions - View all
Common terms and phrases
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