Team:Cornell/Week 11
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August 14th - August 20th
Sunday, August 14
Afternoon lab work done by: Charlie Chung
- Picked three colonies from the two (GFP + Avi-Tagged pZE12 backbone) plates
- - GFP + Avi + BB (1) #1, 2, 3
- - GFP + Avi + BB (2) #1, 2, 3
- Incubating overnight in 37°C shaker of Room 304
- Re-picked three colonies from the (RFP + Avi-Tagged pZE12 backbone) plate in order to retry subculturing, induction, and cell lysis
- - RFP + Avi + BB #7, 8, 9
- Incubating overnight in 37°C shaker of Room 304
Monday, August 15
Afternoon lab work done by: Youjin Cho, Maneesh Gupta
- Objective
- Miniprep GFP samples that were cultured overnight and send them off for sequencing.
- Set-up the PCR for vioB using vio operon.
- Miniprep & Sequencing
- Miniprepped the GFP samples using standard Qiagen Miniprep protocol.
- GFP+Avi-Tag+pZE12 backbone (1)- 1,2,3
- GFP+Avi-Tag+pZE12 backbone (2)- 1,2,3
- Set-up the samples for sequencing using the reverse primer.
- Order number: 10254977
- PCR Reaction
- Set-up the vioB PCR using the vio operon (= 20.3ng/μL).
- As Didi suggested, used the melting temperature of 53°C and annealing time for 3:30 minutes.
Evening lab work done by: Maneesh Gupta, Charlie Chung
Preparing a Subculture
* Set up two cuvettes for preliminary optical density (OD) reading: (1) control (2) RFP sample from Thursday evening
- Purpose of preliminary OD reading is to determine how much RFP sample you need to add to a new 25mL culture - Use a 1:10 dilution of sample to minimize error when running the spectrophotometer
* Control: 1000µL LB * RFP Sample: 900µL LB + 100µL (RFP + Avi-Tagged pZE12) Colony #5
* RFP Sample OD = 0.283 (treat as [bacteria with RFP]), which translates to actual OD of 2.83 in Thursday's 5mL culture tube (after undoing the 1:10 dilution)
* Use dilution equation to determine how much RFP bacteria culture is needed for the 25mL culture
(2.83)(? µL) = (desired beginning [RFP bacteria] = 0.05)(25mL = 25000µL) ? = 441.7µL Thursday's RFP bacteria culture to 25mL LB + 25µL ampicillin
* Incubate new 25mL RFP bacteria subculture in 37°C shaker for ~2 hours and 45 minutes * At end of incubation time, check OD. Target OD = 0.6-0.8, which means ready for induction of RFP production via IPTG * Induce 25mL RFP bacteria culture with 25µL 1M IPTG for desired 1mM addition (completed at 7:25pm) * Incubate induced 25mL culture flask on room temperature shaker