Klapperich Lab:Notebook/Lab Meeting Notes/2008/11/18: Difference between revisions
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==18 November 2008 Lab Meeting Agenda== | ==18 November 2008 Lab Meeting Agenda== | ||
† | † Alex's research report today. | ||
† Announcements<br> | † Announcements<br> | ||
* | * Room 720 move out. <br> | ||
<br> | <br> | ||
† Flu R01 <br> | † Flu R01 <br> | ||
* | * First samples taken starting tomorrow, 11/19. <br> | ||
* Plaque | * Plaque Assay? <br> | ||
* Mark - status of fixture? <br> | * Mark - status of fixture? <br> | ||
<br> | <br> | ||
† SEPSIS Project - CIMIT Bird Flu <br> | † SEPSIS Project - CIMIT Bird Flu <br> | ||
* Cathie working on paper.<br> | * Cathie STILL working on paper.<br> | ||
<br> | <br> | ||
†RNA project | †RNA project | ||
* Jeff Braman will visit | * Jeff Braman will visit December 12th <br> | ||
* Do cDNA prep. Spec, gels, send to Jeff B. Shipping? <br> | * Do cDNA prep. Spec, gels, send to Jeff B. Shipping? <br> | ||
<br> | <br> | ||
† COBRA <br> | † COBRA <br> | ||
* Mark- Control circuit? <br> | * Mark- Control circuit? <br> | ||
* Bacteria Experiment - Changing | * Bacteria Experiment - Changing channel size? <br> | ||
* Substrates ? <br> | |||
* Substrates | |||
<br> | <br> | ||
† Valve Array/Valve building (FJ) <br> | † Valve Array/Valve building (FJ) <br> | ||
* Status from Mark? - valves in transit somewhere. <br> | * Status from Mark? - valves in transit somewhere. <br> | ||
* | * <br> | ||
* | * <br> | ||
<br> | <br> | ||
† Fraunhofer: LOAC <br> | † Fraunhofer: LOAC <br> | ||
* | * <br> | ||
* <br> | * <br> | ||
<br> | <br> | ||
† Biointerfaces group <br> | † Biointerfaces group <br> | ||
* Mask made. Chrome mask. <br> | * Mask made. Chrome mask. <br> | ||
* | * E. Coli experiments with fluorescence? <br> | ||
<br> | <br> | ||
† CIMIT- Colson Grant<br> | † CIMIT- Colson Grant<br> | ||
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<br> | <br> | ||
† PCR <br> | † PCR <br> | ||
* Cathie | * Cathie's flu assay has nonspecific products, too. <br> | ||
* Improve the gel concentration 1.2% agarose. See if you can separate out primer dimers.<br> | * Improve the gel concentration 1.2% agarose. See if you can separate out primer dimers. UPDATE?<br> | ||
* Look into Melting temp analysis on the 7300 - can only do with Sonali's assay. <br> | * Look into Melting temp analysis on the 7300 - can only do with Sonali's assay. <br> | ||
* Only 1/5 chips are good at the hot embossing step. The vaccum chuck will be checked and o-rings changed - helped a bit. <br> | * Only 1/5 chips are good at the hot embossing step. The vaccum chuck will be checked and o-rings changed - helped a bit. <br> | ||
'''* Fixuture for PCR chip. The heater and the thermocouples would be on the fixture. <br>''' | '''* Fixuture for PCR chip. The heater and the thermocouples would be on the fixture. <br>''' | ||
* | * Designed new lambda phage assay with longer product. <br> | ||
* | * What do we need to finish the paper? <br> | ||
* Mincheol will work on DNA migration simulation after IMECE 2008.<br> | * Mincheol will work on DNA migration simulation after IMECE 2008.<br> | ||
<br> | <br> | ||
Line 69: | Line 68: | ||
<br> | <br> | ||
† F31: Cochlea <br> | † F31: Cochlea <br> | ||
* | * Submit paper. <br> | ||
* | * | ||
<br> | <br> | ||
† Silica Optimization (Lambda): <br> | † Silica Optimization (Lambda): <br> | ||
* UPDATE? <br> | |||
* De-inhibit Methyl Methacrylate (100ml), put in fridge, make new columns. <br> | * De-inhibit Methyl Methacrylate (100ml), put in fridge, make new columns. <br> | ||
* Ongoing. More concentrations. <br> | * Ongoing. More concentrations. <br> |
Revision as of 09:14, 18 November 2008
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18 November 2008 Lab Meeting Agenda† Alex's research report today. † Announcements
† COBRA
* Fixuture for PCR chip. The heater and the thermocouples would be on the fixture.
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