Team:UNIPV-Pavia/Methods Materials/Transformation

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     <font face="Pristina" size="50" ><b>Protocols</b></font>
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*Put 1-2 µl of DNA resuspension or ligation into TOP10 tube.
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*Put 1-2 µl of DNA resuspension or ligation into thaw TOP10 cells tube (every tube contains approximately 60 µl of competent cells).
*Incubate on ice for 30 min.
*Incubate on ice for 30 min.
*Heat shock: 42°C for 1 min.
*Heat shock: 42°C for 1 min.
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*Incubate overnight at 37°C.
*Incubate overnight at 37°C.
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<tr bgcolor='yellow'><td>INGREDIENTS:
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*'''LB agar plates with proper antibiotic added incubated at 37°C'''
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*'''Thawed Invitrogen TOP10 cells (every tube contains approximately 60 µl of competent cells)'''
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'''LB agar plates with proper antibiotic'''<hr color='white' width='70%'>
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*'''Resuspended DNA'''
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'''Invitrogen TOP10 cells'''<hr color='white' width='70%'>
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*'''SOC medium'''
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'''SOC medium'''</font>
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Latest revision as of 10:26, 21 October 2009

EthanolPVanimation.gif



Protocols


Transformation

(estimated time: 3 hours and 30 min + 12-16 hours overnight incubation)

  • Put 1-2 µl of DNA resuspension or ligation into thaw TOP10 cells tube (every tube contains approximately 60 µl of competent cells).
  • Incubate on ice for 30 min.
  • Heat shock: 42°C for 1 min.
  • Put transformed TOP10 tube on ice and then add 250 µl SOC medium.
  • Incubate 1 hour at 37°C, 220 rpm.
  • Plate 200 µl of the solution on a proper agar plate.
  • Incubate overnight at 37°C.








INGREDIENTS:

LB agar plates with proper antibiotic
Invitrogen TOP10 cells
Resuspended DNA

SOC medium





Retrieved from "http://2009.igem.org/Team:UNIPV-Pavia/Methods_Materials/Transformation"