Team:DTU-Denmark/Methods/USER Cloning and Transformation

From 2013.igem.org

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(Created page with "===Materials=== PCR product(s) 10X diluted BSA NEB buffer 4 USER enzyme 1 PCR tube/reaction 1 Eppendorf tube/reaction 100 uL competent E.coli/reaction 1 LB-AMP plate/reaction Dri...")
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===Procedure===
===Procedure===
#Label 1,5 mL Eppendorf tubes and place in freezer, remove LB-Amp plates from fridge and place at room temperature.
#Label 1,5 mL Eppendorf tubes and place in freezer, remove LB-Amp plates from fridge and place at room temperature.
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#Mix the USER cloning (<sup>TM</sup>)
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#Mix the USER cloning <sup>TM</sup>

Revision as of 12:22, 6 September 2013

Materials

PCR product(s) 10X diluted BSA NEB buffer 4 USER enzyme 1 PCR tube/reaction 1 Eppendorf tube/reaction 100 uL competent E.coli/reaction 1 LB-AMP plate/reaction Drigalsky's spatchula or sterile glass beads Milli-Q water 96% Ethanol Gas Burner

Procedure

  1. Label 1,5 mL Eppendorf tubes and place in freezer, remove LB-Amp plates from fridge and place at room temperature.
  2. Mix the USER cloning TM