Klapperich Lab:Notebook/Lab Meeting Notes/2009/08/25: Difference between revisions
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* Figures discussion. <br> | * Figures discussion. <br> | ||
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† Silica Optimization (Lambda): <br> | * PATH Grant <br> | ||
* Frank J. | |||
* 12 mos, 24 mos. working prototypes of SNAP. <br> | |||
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† Silica Optimization (Lambda): (get absorbed into the flu agenda item at top) <br> | |||
* August-18-presentation [http://openwetware.org/wiki/Image:Aug_18_09_presentation.ppt] | * August-18-presentation [http://openwetware.org/wiki/Image:Aug_18_09_presentation.ppt] | ||
* Results Summary of Aug-18-09 [http://openwetware.org/wiki/Image:Results_Summary_Aug-18-09.xls] <br> | * Results Summary of Aug-18-09 [http://openwetware.org/wiki/Image:Results_Summary_Aug-18-09.xls] <br> |
Revision as of 08:14, 25 August 2009
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25 August 2009 Lab Meeting
† Flu R01
* Need to update IBC to include rDNA work.
The current problem is not how to visualize virus right now, because the design is clearly not optimized for collecting all the samples at the outlet. The major loss is from sample handling instead of from non specific binding to the material. † Coulter Flu Fraunhofer Project (minor item on new agenda)
* set up 2 week check in meeting with team.
* on-chip PCR on a series of diluted lambda phage DNA. the detect limitation for ABI is 10-9g/ul on-chip PCR have the same sensitivity. * With new syring and tubing, on-chip PCR for the patient sample does not have detectable amplified product. however, the postitive control on the thermal cycle works good.
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