ISISBio:Internal/Group meetings/13-June-08: Difference between revisions
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(New page: Safety Issues: *Autoclave is currently being quoted for plumbing in which seems to be getting out of hand from a cost perspective. *Up to two days disruption to fit tank in ceiling *Query ...) |
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Latest revision as of 04:31, 13 June 2008
Safety Issues:
- Autoclave is currently being quoted for plumbing in which seems to be getting out of hand from a cost perspective.
- Up to two days disruption to fit tank in ceiling
- Query over status of bunsen burner, some suggestion that it needs to be protected and clamped down. This isn't really practical.
- Use of chloroform to clean troughs
- Action LW to ask for risk assessment for trough use
Current Projects Status:
- Preparation of protein for QENS
- MT - lots of GFP available, needs to be purified by gel filtration in advance of beamtime
- Need to not spend too much more time on this
- Action CN to confirm with MT when the beamtime is, prefer September
- Preparation of mellitin for VGS
- Currently checking to see whether initial plasmid has been made
- Several more mol biol steps to go
- Action LW to follow through with next steps
- OmpF for SAH
- LC has purified significant quantities of OmpF, total of about 6 mg
- Played around with making vesicles. PE doesn't make very good vesicles so need to move 25:25:50 PE:PG:PC vesicles
- Going to Oak Ridge for two weeks from 29 June -9 July to deuterate OmpF for SANS experiments
- May need to 5mL DEAE column to Oak ridge for final wash stage
- External reflection IR and DLS organised to do at Reading
- Ion channels
- Currently trying to purify MLok1 in large quantities for ILL on 19 July
- Recent issues with funny bands on gels which seemed to appear in last two weeks. Checking batches against each other.
- Some sample to take but possibly not as much as we want. Would like 3mg/mL for 5/6 contrasts.
- Will also take some mthK to ILL to see whether can see change on addition of Ca2+
- Fluorescent labelling
- Think Michael had made pcr product,now need to purify and ligate to make plasmid
Next week
- Luke using big FPLC all week
- CN/Maria to use baby Akta end of week (Wed-Fri) probably
- MS preparing and transforming Mlok1-LPETGG plasmid and recloning sortase
- VGS probably continuing with mol biol
Week after
- Dave Barlow/Damian experiment to express and purify GlpF/DCytB
- Action CN to contact DB and suggest moving schedule up to avoid Thursday
Logistics
- Need emergency protocol for MCR
- Booking system for lab and equipment