Team:Carnegie Mellon/Met-Protocols

From 2012.igem.org

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<tr> <td width = "25"> 1. </td><td width = "100">Wash 1mL induced cells once with PBS and resuspend in 1mL M9 media.</td></tr>
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<tr> <td width = "25"> 1. </td><td width = "200">Wash 1mL induced cells once with PBS and resuspend in 1mL M9 media.</td></tr>
<tr><td>2. </td><td>Add 1µL of 50nM Mg2+ as MgCl2 from PCR kit to the tubes</td></tr>
<tr><td>2. </td><td>Add 1µL of 50nM Mg2+ as MgCl2 from PCR kit to the tubes</td></tr>
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Revision as of 03:11, 17 September 2012

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Protocols

Overview

Our protocols are based on standard lab protocols used in the lab of our advisers unless otherwise stated. These protocols were subsequently modified if necessary based on our experience. A knowledge of basic lab techniques such as pippeting, plating, etc. are assumed and not covered as there are pretty comprehensive tutorials on the web for those.

Dosage Curve

1. Wash 1mL induced cells once with PBS and resuspend in 1mL M9 media.
2. Add 1µL of 50nM Mg2+ as MgCl2 from PCR kit to the tubes

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