IGEM:MIT/2007/Notebook/2007-7-10
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Agenda
- Red Team - Meeting Friday 11am w/ Drew and Tom
- Metal Contacts
- email Meinke
- email Cad grad (mark.ensor@uky.edu)
- email/call pUT-Mer - Copenhagen
- Send for sequencing: miniprep of F2620, E1010, B0034
- design/order Mer Primers
- design/order FhuA Primers
- High Copy Plasmids
- Transform MerPR+MerR plasmids
- competent cells - Tom?
- Obtaining untreated polystyrene for filter
Checked Transformation Plates
DH5a in Amp (100µl) - 14 colonies DH5a in Amp (300µl) - 60 DH5a in Kan (100µl) - 4 DH5a in Kan (300µl) - 10 XL-1 in Amp (20µl) - 720 colonies XL-1 in Amp (200µl) - 4800 XL-1 in Kan (20µl) - 220 XL-1 in Kan (300µl) - 800
Innoculated 4 Liquid Cultures of Transformation from XL-1 in Kan (20µl) Plate
- Used 5ml of LB+Kan
- Placed in 37C room at around 12pm
Sent out F2620, B0034, E1010 for Sequencing
- Used samples #2 because those were also used for the digestion/ligation/3A
- Form 7942
- Used 3µl of each miniprepped DNA sample, 1µl of VF2/VR, and 8µl H2O (12µl total)