Team:Brown-Stanford/Lab/Protocols/CementationColumn
From 2011.igem.org
(Difference between revisions)
Maxsong123 (Talk | contribs) (→Materials) |
|||
Line 1: | Line 1: | ||
{{:Team:Brown-Stanford/Templates/Main}} | {{:Team:Brown-Stanford/Templates/Main}} | ||
- | + | <html> | |
+ | <div id="subHeader"> | ||
+ | <ul id="subHeaderList"> | ||
+ | <li><a href="/Team:Brown-Stanford/Team">Team</a></li> | ||
+ | <li><a href="/Team:Brown-Stanford/Lab/Notebook">Notebook</a></li> | ||
+ | <li id="active"><a href="#" id="current">Protocols</a></li> | ||
+ | <li><a href="/Team:Brown-Stanford/Lab/Safety">Safety</a></li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </html> | ||
+ | {{:Team:Brown-Stanford/Templates/Content}} | ||
== '''Biocementation Column''' == | == '''Biocementation Column''' == | ||
Revision as of 17:40, 27 September 2011
Biocementation Column
Materials
- 15 mL falcon tube
- 20 g of Lunar/Martian regolith per tube
- A peristaltic pump
- Two feet of rubber tubing, epoxy glue, fabric matting
- Heat Lamp
- 30 mL of S. pasteurii culture (OD600 1.2)
Procedure
- The columns were first prewet with 20 mL of sterile Bang media.
- The bacteria culture was draw into the feed tube, and allowed to settle in the column overnight
- Cementation solution (1.5 M equimolar urea and calcium chloride) was fed into the feed tube, which was then placed into a constant loop with the output tube
- The column was heated for 5 days, and allowed to cycle.