Team:Calgary/Notebook/Protocols/GlassBeadsCellLysisProtocolforProteinSamples
From 2013.igem.org
(Difference between revisions)
(Created page with "<html> <div id="Banner"><h1>Glass Beads Cell Lysis Protocol</h1></div> </html> {{Team:Calgary/ContentPage}} <html> <section id="Content"> <h1>Glass Beads Cell Lysis Protocol for ...") |
Sharonfeng1 (Talk | contribs) |
||
Line 10: | Line 10: | ||
<ul> | <ul> | ||
<li>0.1m diameter glass beads</li> | <li>0.1m diameter glass beads</li> | ||
- | <li>Lysis | + | <li>Lysis buffer </li> |
<li>Overnight induced cultures</li> | <li>Overnight induced cultures</li> | ||
<li>1.5mL tubes</li> | <li>1.5mL tubes</li> |
Revision as of 23:17, 27 September 2013
Glass Beads Cell Lysis Protocol
Glass Beads Cell Lysis Protocol for Protein Samples
Reagents and Materials
- 0.1m diameter glass beads
- Lysis buffer
- Overnight induced cultures
- 1.5mL tubes
Protocol
- Culture and induce protein-producing bacteria
- Centrifuge cells at max for 10 minutes. Discard supernatant
- Resuspend cells in 2mL of lysis buffer
- In a 1.5mL tube, add ~0.5mL of glass beads and 1mL of cells resuspended in lysis buffer
- Leave on ice for 5 min. Leave on BeadBeater or Vortex for 5 min. Repeat this cycle 6 times
- Centrifuge at max for 20 minutes
- Transfer supernatant (crude lysate) to a new tube and discard the glass beads