Klapperich Lab:Notebook/Lab Meeting Notes/2009/11/24: Difference between revisions
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† HDA (Lead: Jaephil, Team:Sonali)<br> | † HDA (Lead: Jaephil, Team:Sonali)<br> | ||
* Start planning R01 for Submission on 2/5/10. MM, JD, CMK. <br> | * Start planning R01 for Submission on 2/5/10. MM, JD, CMK. <br> | ||
* Dry reagent storage for RT and HDA - COP test well array provided fo Sonali <br> | * Dry reagent storage for RT and HDA - COP test well array provided fo Sonali <br> | ||
* Set-up meeting for 2nd HDA design - Target (Flu or Bacteria), include RT or not, Heat source, address evaporation loss, Reagent delivery and storage solution. Consider marginating flows and include RT? <br> | * Set-up meeting for 2nd HDA design - Target (Flu or Bacteria), include RT or not, Heat source, address evaporation loss, Reagent delivery and storage solution. Consider marginating flows and include RT? <br> | ||
* Paper resubmission. <br> | * Paper resubmission. Cathie will do Wed. <br> | ||
<br> | <br> | ||
† Sample Concentration (Lead: Jane, Team: Jaephil) <br> | † Sample Concentration (Lead: Jane, Team: Jaephil) <br> | ||
* New design sent to make Rubber mold: outline octagon problem. Revised design sent yesterday. <br> | * New design sent to make Rubber mold: outline octagon problem. Revised design sent yesterday. <br> | ||
* Jane will train Cassidy once more on Wednesday and Thursday this week. <br> | * Jane will train Cassidy once more on Wednesday and Thursday this week. <br> | ||
** MM 040808 A/PR/8/34 flu stock with PFU = 2X10^4 available to Jane to train Cassidy in ultracentrifuging all tubes <br> | ** MM 040808 A/PR/8/34 flu stock with PFU = 2X10^4 available to Jane to train Cassidy in ultracentrifuging all tubes <br> | ||
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* Set up COMSOL and StarCD, look for governing equations for simulation of evaporation. - ongoing <br> | * Set up COMSOL and StarCD, look for governing equations for simulation of evaporation. - ongoing <br> | ||
<br> | <br> | ||
† SPE Column Optimization for RNA. (Lead: Sonali, Team: Hussam, Jessie, Brendan) <br> | † SPE Column Optimization for RNA. (Lead: Sonali, Team: Hussam, Jessie, Brendan) <br> | ||
*pH the sample. Optimum 6.6. Make sure that we are there. 3M GUSCN stands at pH 4.2 very acidic (some NaOH)<br> | *pH the sample. Optimum 6.6. Make sure that we are there. 3M GUSCN stands at pH 4.2 very acidic (some NaOH)<br> | ||
* | * "Measure again 1:1 with DEPC water, 1:1 with PBS" | ||
* | * Silica nanoparticles from Fluka. 15nm "order"<br> | ||
*Still working on the 150nm particles 1X experiments<br> | *Still working on the 150nm particles 1X experiments with lambda. HM<br> | ||
<br> | <br> | ||
*PLanning net silica per channel experiments. with 700nm, 3x possible. Deliver around 11/5/09.<br> | *PLanning net silica per channel experiments. with 700nm, 3x possible. Deliver around 11/5/09.<br> | ||
<br> | <br> | ||
* 150nm and 700nm silica with 0.5mm (3.6uL SPE) channels.<br> | * 150nm and 700nm silica with 0.5mm (3.6uL SPE) channels.<br> | ||
* 150nm Silica did not improve Ct on average, but one channel with 700nm silica performed exceptionally well, which brought the average up.<br> | * 150nm Silica did not improve Ct on average, but one channel with 700nm silica performed exceptionally well, which brought the average up.<br> | ||
*"relationship between PFU/ml and copy # of RNA. Do this via a serial dilution of Virus, put through Qiagen kit. Assuming that Qiagen is 100% efficient." <br> | |||
* "Jessie get trained for real on SEM.*"<br> | |||
† PCR - CMI (Lead: Qingqing) <br> | † PCR - CMI (Lead: Qingqing) <br> | ||
* QQ will work on the initial integration steps of SPE + RT (reservoir)+ PCR. <br> | * QQ will work on the initial integration steps of SPE + RT (reservoir)+ PCR. <br> | ||
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'''‡ Coulter Flu Fraunhofer Project (Lead: Sonali, Team: Sonali, Jessie, Cathie, CMI Folks, Qingqing)''' | '''‡ Coulter Flu Fraunhofer Project (Lead: Sonali, Team: Sonali, Jessie, Cathie, CMI Folks, Qingqing)''' | ||
* Meeting 9am Monday (every other week) <br> | * Meeting 9am Monday (every other week) <br> | ||
* | * "ASB will give action items." <br> | ||
<br> | <br> | ||
'''‡ Agilent Automated Sample Preparation (Lead: Alex)'''<br> | '''‡ Agilent Automated Sample Preparation (Lead: Alex)'''<br> | ||
* So far tested on SNAP2: <br> | * So far tested on SNAP2: <br> | ||
** B. subtilis gDNA <br> | ** B. subtilis gDNA <br> | ||
** B. subtilis cells <br> | ** B. subtilis cells, high Cts for the range tested. <br> | ||
* Planned tests SNAP2: <br> | * Planned tests SNAP2: <br> | ||
** B. subtilis cells (higher concentrations) <br> | ** B. subtilis cells (higher concentrations) <br> | ||
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* Paper on Yeast: Extended Literature Review (12/11) <br> | * Paper on Yeast: Extended Literature Review (12/11) <br> | ||
* PATH: straw holder for Blackbird is machined <br> | * PATH: straw holder for Blackbird is machined <br> | ||
'''‡ COBRA (Lead: Jaephil, Team: Cathie, Jane for virus only, PHO folks)<br>''' | '''‡ COBRA (Lead: Jaephil, Team: Cathie, Jane for virus only, PHO folks)<br>''' | ||
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* Cathie submitted the companion BU IRB form for exemption. Revised, still still waiting. <br> | * Cathie submitted the companion BU IRB form for exemption. Revised, still still waiting. <br> | ||
<br> | <br> | ||
'''‡ PATH Grant (Lead:Cathie, Team:Frank, Sean, Mark, Jake Trueb (ME) | '''‡ PATH Grant (Lead:Cathie, Team:Frank, Sean, Mark, Jake Trueb (ME))''' <br> | ||
* Phone meeting with PATH this week. 10/13. <br> | * Phone meeting with PATH this week. 10/13. <br> | ||
* Senior Project Proposals submitted; proposal presentations Friday after Thanksgiving (Dec. 4).<br> | * Senior Project Proposals submitted; proposal presentations Friday after Thanksgiving (Dec. 4).<br> | ||
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* Sean met with Alex for an integration of straws on black machine. They sketched a design. Sean will make a professional drawing and create a required parts list. Alex will supervise the design. Before handing in the job to the shop floor, the design will be presented to Cathie. <br> | * Sean met with Alex for an integration of straws on black machine. They sketched a design. Sean will make a professional drawing and create a required parts list. Alex will supervise the design. Before handing in the job to the shop floor, the design will be presented to Cathie. <br> | ||
* Mark to begin initial DNA testing with shorter time periods (1,3 days, etc.) to be completed this(?) week. PCR training completed. Ready to begin testing. Waiting for new straw fixture to be ready for testing (where will it be stationed?). <br> | * Mark to begin initial DNA testing with shorter time periods (1,3 days, etc.) to be completed this(?) week. PCR training completed. Ready to begin testing. Waiting for new straw fixture to be ready for testing (where will it be stationed?). <br> | ||
<br> | |||
‡IIH Senior Project. | |||
* Trouble locating PMMA sheet. <br> | |||
* Try Dow Chemical Website. FOOD safe, FDA grade. <br> | |||
Revision as of 13:20, 24 November 2009
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24 November 2009 Lab Meeting
‡ Announcements
† HDA (Lead: Jaephil, Team:Sonali)
† SPE Column Optimization for RNA. (Lead: Sonali, Team: Hussam, Jessie, Brendan)
† PCR - CMI (Lead: Qingqing)
- SPE+RT+PCR chip is designed.
- toxin A. HDA assay for toxin A is tested in tube. It works HDA chip will be designed, and tested. SPE DNA from lisa for test? - toxin B. on chip PCR works.
need to get back from Cathie
‡ COBRA (Lead: Jaephil, Team: Cathie, Jane for virus only, PHO folks)
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