To Do
- Autoclave stuff today!
- Pipette tips (1000ul) that fell out, they are sitting in the autoclave
- More centrifuge tubes (the large ones)
- Popin buffer
- More BNC Cables
- OT?
Autoclaving
- When I came in, the Autoclave was in use
- Andy says that Nathan (Osinski's Lab) was using it
- Round one (probably the only round since our group meeting is today)
- 1x 1000ul tips (the ones i got dirty Friday)
- 2x 100ul tips
- 5x large centrifuge tips
- Note: I went ahead and autoclaved ALL of the tubes in the plastic bag since we only had 1 more container of them and I wanted to make sure we had some in reserve
- Round 2
BNC
- Whilst waiting for the Autoclave, I will make some 3ft and 4 ft BNC cables
- one 4ft made friday, one made today
- two 3ft made today
New Lab Network
- Used Koch's laptop to check the 4 ports that are in the new lab (2 at front door 2 at rear door)
- They all provided me with internet access and I was able to access //controller
- I will take down the annoying wire tomorrow since today I need to read up on the paper for the meeting
OT
- Koch, Ant and I tethered some DNA and tried unzipping
- There is a problem with the translator/piezzo
- They seem to be misaligned because we get alot of "sliding"
- Ex. the x translation works fine, but when you use the Y translator it has a diagonal movement wrt the microscope plane
- We were able to find some tethers and pull on them
- We feel that the trap is too weak since the beads keep coming out of the trap
- it could also be a problem with the piezzo (misaligned and/or moving too fast)
- Good note: 500nm beads are easy to see and very easily trapped (sometimes we get them when we dont want them)
- We need to calibrate the tweezers tomorrow
- Cool note: I think i saw dna unzip, but that result was unrepeatable
- We turned on the trap near a tether, saw it move, then turned off the trap.
- The bead "sprung back" to its original spot and oscillated a bit (like a block on a spring)
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