Pathogen corruption and site-directed recombination at a plant disease resistance gene cluster

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Figure 3.
Figure 3.

Expression analysis on susceptible Colby (Pc) and nine derived pc isolines using RT-PCR. A primer pair common to all three NBS–LRR paralogs was used. Negative controls (C.), lacking reverse transcriptase in their reaction mixtures, were also included. The PCR products were cloned and sequenced to identify expressed paralogs.

This Article

  1. Genome Res. 18: 1918-1923

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