Team:Columbia-Cooper-NYC/trial

From 2012.igem.org

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<FONT SIZE="+1" COLOR="000000">• Met with Jason, who showed us how to make A. ferrooxidans liquid media, prepared Copper 1 and 2</FONT></DIV>
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<FONT SIZE="+1" COLOR="000000">• Met with Jason, who showed us how to make A. ferrooxidans liquid media, prepared Copper 1</FONT></DIV>
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<FONT SIZE="+1" COLOR="000000"> samples (with and without bacteria) and placed on shaker. Will be periodically checked until June 25</FONT></DIV>
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<FONT SIZE="+1" COLOR="000000"> and 2 samples (with and without bacteria) and placed on shaker. Will be periodically checked until June 25</FONT></DIV>
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Revision as of 20:56, 16 August 2012

Notebook Background.jpg

Copper Experiments 1
Friday, June 22nd
Outline of activity today:
• Met with Jason, who showed us how to make A. ferrooxidans liquid media, prepared Copper 1
and 2 samples (with and without bacteria) and placed on shaker. Will be periodically checked until June 25
twice a day for activity.
• Showed us recipe for solid media, and made enough for two samples, 20 mL (one control with no
bacteria). Copper samples were submerged in agarose (see Steven’s pictures). Also learned protocols
listed below.
Starting Sample masses:
Copper 1: (liquid media only)
Sample Mass (g)
1 0.0092
2 0.0107
Copper 2: (liquid media only)
Sample Mass (g)
1 0.1318
2 0.1286
Copper 2: (solid media)
Sample Mass (g)
1 0.1272
2 0.1282
Liquid media and flasks were placed in shaker at 225 rpm, 30C.
Solid media and petri dishes were placed in incubator at 30C.