Team:UCL London/From the lab/Protocols
From 2009.igem.org
(Difference between revisions)
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# Cf 3300g 5 min in benchtop RmT. Cf. | # Cf 3300g 5 min in benchtop RmT. Cf. | ||
# Resus in 1ml ice cold 0.1M CaCl2 / 15% glycerol. Transfer 100µl aliquots to pre-chilled, pre-labelled eppendorf tubes. Store -80°C. | # Resus in 1ml ice cold 0.1M CaCl2 / 15% glycerol. Transfer 100µl aliquots to pre-chilled, pre-labelled eppendorf tubes. Store -80°C. | ||
+ | |||
+ | |||
+ | ---- | ||
+ | |||
+ | |||
+ | '''Transformation:''' | ||
+ | |||
+ | : '''''Materials:''''' | ||
+ | * Plasmids DNA | ||
+ | * Competent E.coli | ||
+ | * NZY Medium | ||
+ | * LB buffer | ||
+ | * Ampicllin, Kanamycin, Tetracycline | ||
+ | * Agar Plates | ||
+ | * Eppendorf | ||
+ | |||
+ | : '''''Method 1:''''' | ||
+ | # Add 5µL ice-cold plasmid DNA into the competent E.coli on ice. | ||
+ | # Incubate on ice for 30 min. (minimum) Incubate at 42°C for 45 sec. | ||
+ | # Incubate on ice for 2 min. (minimum) | ||
+ | # Add 300µL of NZYX medium. | ||
+ | # Incubate with shaking at 37°C for 1 hr. | ||
+ | # Spin the incubated E.coli suspension for 3min at maximum speed. (Optional) | ||
+ | # Discard about half of the liquid, and then re-suspend the E.coli solution. (Optional) | ||
+ | # Spread the suspension onto selective agar plates. | ||
+ | # Incubate at 37°C overnight. | ||
+ | # Pick a colony into 2ml selective LB (Add 100µL antibiotic to 50mL LB medium). Incubate 37°C in shaker overnight | ||
+ | |||
+ | : '''''Method 2:''''' | ||
+ | # Using the puch tool, puch out the appropriate DNA. Clean the tool between punches. | ||
+ | # Soak the spots in 5µL of TE that has been warmed to 50ºC for 20 minutes. At this time take the competent cells from the -80º freezer and start defrosting on ice. | ||
+ | # Add 2µL of DNA in TE to 50µL of competent cells (TOP10) | ||
+ | # Allow the DNA and competent cells to sit on ice for 30 minutes | ||
+ | # Heat shock at 42ºC for 60 sec in water bath. | ||
+ | # Recover on ice for 5 min. | ||
+ | # Add 200 µL SOC media. | ||
+ | # Incubate at 37ºC for 2 hr while the tubes are rotating. | ||
+ | # Centrifuge and leave about 100 µL liquid; hence, resuspend the E.coli suspension. | ||
+ | # Plate 250µL on an LB plate with the appropriate antibiotic. |
Revision as of 08:57, 6 July 2009
Competent Bacteria:
- Materials:
- 5×M9 salts in 500ml dH2O:
- Na2HPO4--- 32g
- KH2PO4 --- 7.5g
- NaCl --- 1.25g
- NH4Cl --- 2.5g
- Minimal media: ( In 50ml Falcon )
- Melted bacteriological agar solution (< 50°C) --- 39ml
- 5×M9 salt solution --- 10ml
- 20% (w/v) D-glucose --- 1ml
- 1M CaCl2 --- 5µl
- 1M MgSO4 --- 100µl
- 0.1M CaCl2 / 15% glycerol: (In 59 ml Falcon)
- 1M CaCl2 --- 5ml
- 100% glycerol --- 7.5ml
- Preparation:
- Pour minimal media plates.
- 5x M9 salts.
- Prepare 100ml LB per strain.
- Prepare 50ml ice cold 0.1M CaCl2 / 15% glycerol per strain
- Pre-chill eppendorf tubes
- Method:
- Streak cells on minimal agar plate. Incubate 37°C overnight.
- Pick a colony into 5 ml LB + 100µl 1M MgSO4. Incubate 37°C overnight.
- Inoculate 100ml LB in pre-warmed conical with 1ml of the 5ml O/N culture from Step 2.
- Incubate 2 hrs in 37°C shaker until the cells at early log phase of growth curve (A600 ~ 0.3).
- Transfer to chilled, sterile two 50ml Falcon tubes and incubate on ice for 10 min.
- Cf 3300g 5 min in bechtop RmT. Cf.
- Resus in 10ml ice cold 0.1M CaCl2 / 15% glycerol and incubate on ice 30 min.
- Cf 3300g 5 min in benchtop RmT. Cf.
- Resus in 1ml ice cold 0.1M CaCl2 / 15% glycerol. Transfer 100µl aliquots to pre-chilled, pre-labelled eppendorf tubes. Store -80°C.
Transformation:
- Materials:
- Plasmids DNA
- Competent E.coli
- NZY Medium
- LB buffer
- Ampicllin, Kanamycin, Tetracycline
- Agar Plates
- Eppendorf
- Method 1:
- Add 5µL ice-cold plasmid DNA into the competent E.coli on ice.
- Incubate on ice for 30 min. (minimum) Incubate at 42°C for 45 sec.
- Incubate on ice for 2 min. (minimum)
- Add 300µL of NZYX medium.
- Incubate with shaking at 37°C for 1 hr.
- Spin the incubated E.coli suspension for 3min at maximum speed. (Optional)
- Discard about half of the liquid, and then re-suspend the E.coli solution. (Optional)
- Spread the suspension onto selective agar plates.
- Incubate at 37°C overnight.
- Pick a colony into 2ml selective LB (Add 100µL antibiotic to 50mL LB medium). Incubate 37°C in shaker overnight
- Method 2:
- Using the puch tool, puch out the appropriate DNA. Clean the tool between punches.
- Soak the spots in 5µL of TE that has been warmed to 50ºC for 20 minutes. At this time take the competent cells from the -80º freezer and start defrosting on ice.
- Add 2µL of DNA in TE to 50µL of competent cells (TOP10)
- Allow the DNA and competent cells to sit on ice for 30 minutes
- Heat shock at 42ºC for 60 sec in water bath.
- Recover on ice for 5 min.
- Add 200 µL SOC media.
- Incubate at 37ºC for 2 hr while the tubes are rotating.
- Centrifuge and leave about 100 µL liquid; hence, resuspend the E.coli suspension.
- Plate 250µL on an LB plate with the appropriate antibiotic.