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. Author manuscript; available in PMC: 2011 Aug 16.
Published in final edited form as: Methods Mol Biol. 2009;535:135–163. doi: 10.1007/978-1-59745-557-2_9

Fig. 9.6.

Fig. 9.6

Recombinant PCR as a means of generating a DNA fragment for use as a transcription template without the need for cloning. (A) Schematic of the PCR reactions needed to generate a full length fragment for transcription. Reactions 1a, 1b, and 1c are analogous to the reactions outlined in Sections 3.3.1, 3.3.2, and 3.3.3, respectively. (B) Ethidium bromide stained gel showing fragments generated in Step 1 (lane a, b) and Step 2 (lane c) of the scheme.