File:Site-directed mutagenesis library cloning steps.pdf

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English: Depiction of one common way to clone a site-directed mutagenesis library (i.e., using degenerate oligos). The gene of interest is PCRed with oligos that contain a region that is perfectly complementary to the template (blue), and one that differs from the template by one or more nucleotides (red). Many such primers containing degeneracy in the non-complementary region are pooled into the same PCR, resulting in many different PCR products with different mutations in that region (individual mutants shown with different colors below).
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Source Own work
Author Rob Hurt

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Site-directed mutagenesis library cloning steps

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6 April 2020

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current20:57, 6 April 2020Thumbnail for version as of 20:57, 6 April 20201,687 × 937 (394 KB)Rob HurtUploaded own work with UploadWizard
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