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. Author manuscript; available in PMC: 2010 Mar 23.
Published in final edited form as: Methods Mol Biol. 2009;504:441–458. doi: 10.1007/978-1-60327-569-9_24

Fig. 5.

Fig. 5

Amplification of Shigella dysenteriae DNA using the single channel TFRT. PCR amplification (35 cycles) of ipaH gene from Shigella dysenteriae on a conventional Peltier-based thermocycler and thin-film resistive thermocycler (TFRT) in a single-capillary mode. (A) gel, (B) capillaries. M – 123 bp DNA ladder (see Note 10), 1 – negative control, 2 – TFRT (37 min), 3 – TFRT (20 min), 4 – TFRT (17.5 min), 5 – Conventional thermocycler (122 min).