File:2013 CUBoulder gel.png

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The CU-Boulder 2013 team worked on a low-cost restriction enzyme expression and purification system optimized for minimal equipment and reagents use to enable simple, on-location production of BBF10-compatible REs while reducing waste flows. This led the team to demonstrate several clever shortcuts for routine molecular biology techniques, such as a protein purification protocol using an agarose gel and enzyme purification with elastin fusion proteins. Overall, their project demonstrated affordable alternatives to more costly techniques that are often taken for granted in traditional settings.

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current04:52, 9 April 2015Thumbnail for version as of 04:52, 9 April 2015600 × 234 (121 KB)Macowell (Talk | contribs)The CU-Boulder 2013 team worked on a low-cost restriction enzyme expression and purification system optimized for minimal equipment and reagents use to enable simple, on-location production of BBF10-compatible REs while reducing waste flows. This led the

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