Wisconsin: Lignin Project/1 July 2008

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Team Sorbitol

The overnight PCR reaction failed.

Used the purified PCR product from yesterday to set up a digestion (along with pBAD30) as described before.

The digestion was verified on a gel and extracted using the Qiagen kit.

This time we obtained enough insert to do a ligation but not enough vector.

To solve this we grew 40mL of DH5a with pBAD30 overnight at 30C