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Template:Team:KULeuven/15 September 2009/VanillinReceptor
From 2009.igem.org
- Because virA was now properly inserted in the pucvector we could now start mutagenesis on restriction sites 187 and 720. We did this with PCR. We used a protocol for site-directed-mutagenesis with the matching primers. PCR was done overnight
- new ligation for virB was done
