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Verification of 99 primer pairs for non-OR genes using qPCR analysis. The target genes were randomly selected from among non-OR genes (including pheromone receptors, G proteins, ion channels, signaling molecules and so on) in the mouse CCDS database. We used the top-1 primer pair automatically designed by MRPrimer. PCR amplification and amplicon dissociation analyses were performed successfully. (A) Amplification curves of the target genes. (B) Melting curves of the target genes.
