Difference between revisions of "Team:Freiburg/Protocols/Bead Regeneration"
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Latest revision as of 08:55, 10 September 2015
Ni-NTA bead regeneration
LP to regenerate Ni-NTA beads after use and elution of bound proteins
- centrifuge beads in Lysis buffer 1 min @ 500 g, 4°C
- discard supernatant
- add 2 mL 0.5 M NaOH per 15 mL Falcon tube
- resuspend beads by flicking against the tube
- incubate 30 min on ice
- centrifuge 1 min @ 500 g, 4°C
- discard supernatant
- resuspend beads im 20 % ethanol by flicking
- store @ 4°C