Team:Washington/Protocols/plate expression
From 2011.igem.org
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#Day 1: OVERNIGHTS | #Day 1: OVERNIGHTS | ||
##Pick a single colony from plate and inoculate 0.5ml of room temp LB/Kan (NOT TB) in STERILE deep well plate (Round bottom 2 mL Deepwell plate; e.g. Cat No # 7701-5205) | ##Pick a single colony from plate and inoculate 0.5ml of room temp LB/Kan (NOT TB) in STERILE deep well plate (Round bottom 2 mL Deepwell plate; e.g. Cat No # 7701-5205) |
Latest revision as of 23:10, 28 September 2011
Plate Expression
- Day 1: OVERNIGHTS
- Pick a single colony from plate and inoculate 0.5ml of room temp LB/Kan (NOT TB) in STERILE deep well plate (Round bottom 2 mL Deepwell plate; e.g. Cat No # 7701-5205)
- Generally we have been picking and growing up 4 individual colonies/mutation, so we have quadruplicate data on each mutation. Plate assays have a lot of variability and each colony is not guaranteed to have the mutation, so quadruplicate assaying helps significantly.
- Cover with breathable seal
- Shake at 37deg 16-24hrs in warm room plate shaker (Heidolph Brinkmann Titramax 1000 @ 1200rpm) to ensure they are all fully grown
- Pick a single colony from plate and inoculate 0.5ml of room temp LB/Kan (NOT TB) in STERILE deep well plate (Round bottom 2 mL Deepwell plate; e.g. Cat No # 7701-5205)
- Day 2: EXPRESSION
- Vortex the overnights at 1500rpm for 30sec to ensure to mix any cells that have settled to the bottom into the media.
- Make glycerol stocks if first time doing this set: 110uL cells + 110uL 20% glycerol. Store in -80.
- Inoculate a fresh STERILE plate of 1.0ml of TB/Kan in a deep well plate with 20uL of overnight cultures
- Cover with breathable seal
- Grow at 37deg as above for 3 hours (target OD approx 0.3-0.8)
- Get IPTG out of freezer to defrost for 3 hours - don't let it defrost longer than 3 hours
- Add IPTG to 0.5mM (50uL of 10mM IPTG) using the repeater
- Transfer plate to 18deg shaker (Heidolph Brinkmann Titramax+Incubator 1000 @ 1200rpm in cold room, preheat to 18) and shake at 1200rpm for 24-30hrs.
- Vortex the overnights at 1500rpm for 30sec to ensure to mix any cells that have settled to the bottom into the media.
- Day 3: STORE
- Spin down cells at 4000rpm for 20min
- Pour off supernatant
- Store cells in -20 until ready for purification