Difference between revisions of "A high-throughput capillary assay for bacterial chemotaxis"
(New page: Zach Wissner-Gross (March 2, 2009) ==Information== A high-throughput capillary assay for bacterial chemotaxis Russell Bainer, Heungwon Park, and Phillipe Cluzel Journal of Microbiologic...) |
(→Summary) |
||
| Line 12: | Line 12: | ||
==Summary== | ==Summary== | ||
| + | |||
| + | A methods paper, this article is relatively straightforward. The authors use a 96-well plate to perform a high-throughput assay for bacterial chemotaxis by setting up an array of gradients of L-aspartate (a chemoattractant). They establish these gradients using capillary tubes: first they dipped the tubes into motility medium either with or without the L-aspartate. They then sealed the tubes from above with wax, and finally they resuspended the tubes in 96-well plates inoculated with various bacterial concentrations. | ||
Revision as of 22:02, 1 March 2009
Zach Wissner-Gross (March 2, 2009)
Information
A high-throughput capillary assay for bacterial chemotaxis
Russell Bainer, Heungwon Park, and Phillipe Cluzel
Journal of Microbiological Methods, 2003, 55, 315-319
Soft matter Keywords
E. coli, chemotaxis, capillary
Summary
A methods paper, this article is relatively straightforward. The authors use a 96-well plate to perform a high-throughput assay for bacterial chemotaxis by setting up an array of gradients of L-aspartate (a chemoattractant). They establish these gradients using capillary tubes: first they dipped the tubes into motility medium either with or without the L-aspartate. They then sealed the tubes from above with wax, and finally they resuspended the tubes in 96-well plates inoculated with various bacterial concentrations.
