User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2013/01/21

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(Autocreate 2013/01/21 Entry for User:Behzad_Damadzadeh/Notebook/PcTF_Subcloning_in_E-coli)
Current revision (15:02, 22 January 2013) (view source)
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=Date=
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=01/21/2013=
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=Chemically Competent Cell Prep ''(BL21-DE3)''=
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Haynes Lab, 2013
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'''List title'''
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Prepare these solutions ahead of time and chill at 4°C overnight:<br>
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# List items
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100 mM CaCl<sub>2</sub>, autoclaved<br>
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15% glycerol in sterile 100 mM CaCl<sub>2</sub><br><br>
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* First autoclave the 100mM CaCl<sub>2</sub><br><br> and then make 15% glycerol solution. (Do not autoclave the glycerol)
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# Grow untransformed cells on plain LB (streak for single colonies).
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# Inoculate 12.5 mL culture with colony from plate. Incubate with shaking at 37°C for 8 hours.
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# Prepare two 250 mL of plane LB Broth and autoclave.
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# Transfer 6.2 mL culture into 250 mL. Grow until absorbance of 0.6 A600 is reached. BL21 growth is slow, overnight incubation is recommended. (12hrs)
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# Aliquot 125 mL culture to 4 sterile large 250mL polycarbonate spin bottles. Chill on ice for 15 min.
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# Centrifuge cells at 4000 rpm for 10 min ate 4°C. (Dr. Wang's lab refrigerator centrifuge)
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# Resuspend cells in sterile, ice-cold 100 mM CaCl<sub>2</sub> by gentle pipetting (do not vortex!). Use 37.5 mL per 125mL culture (75 mL per 250 cell culture). Incubate on ice for 15 min.
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# Centrifuge cells at 4000 rpm for 10 min at 4°C.
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# Resuspend in sterile, ice-cold 100 mM CaCl<sub>2</sub>/15% glycerol (do not vortex!). Use 20 mL per 250 mL culture.
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*The cell pellets are very sticky. We need to pipette up and down for a long time to get them completely resuspended.
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# Leave on ice in a cold room/ fridge for 21 hours.
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# Freeze 200μL aliquots of cells in sterile microcentrifuge tubes. Store at -80°C.

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01/21/2013

Chemically Competent Cell Prep (BL21-DE3)

Haynes Lab, 2013

Prepare these solutions ahead of time and chill at 4°C overnight:
100 mM CaCl2, autoclaved
15% glycerol in sterile 100 mM CaCl2

  • First autoclave the 100mM CaCl2

    and then make 15% glycerol solution. (Do not autoclave the glycerol)
  1. Grow untransformed cells on plain LB (streak for single colonies).
  2. Inoculate 12.5 mL culture with colony from plate. Incubate with shaking at 37°C for 8 hours.
  3. Prepare two 250 mL of plane LB Broth and autoclave.
  4. Transfer 6.2 mL culture into 250 mL. Grow until absorbance of 0.6 A600 is reached. BL21 growth is slow, overnight incubation is recommended. (12hrs)
  5. Aliquot 125 mL culture to 4 sterile large 250mL polycarbonate spin bottles. Chill on ice for 15 min.
  6. Centrifuge cells at 4000 rpm for 10 min ate 4°C. (Dr. Wang's lab refrigerator centrifuge)
  7. Resuspend cells in sterile, ice-cold 100 mM CaCl2 by gentle pipetting (do not vortex!). Use 37.5 mL per 125mL culture (75 mL per 250 cell culture). Incubate on ice for 15 min.
  8. Centrifuge cells at 4000 rpm for 10 min at 4°C.
  9. Resuspend in sterile, ice-cold 100 mM CaCl2/15% glycerol (do not vortex!). Use 20 mL per 250 mL culture.
  • The cell pellets are very sticky. We need to pipette up and down for a long time to get them completely resuspended.
  1. Leave on ice in a cold room/ fridge for 21 hours.
  2. Freeze 200μL aliquots of cells in sterile microcentrifuge tubes. Store at -80°C.
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