Figure 2From: Development of one-step TaqMan® real-time reverse transcription-PCR and conventional reverse transcription-PCR assays for the detection of equine rhinitis A and B virusesComparison of detection sensitivity of the three rRT-PCR assays using ERAV or ERBV prototype strains from NVSL (ERAV rRT-PCR assay [ y = 3.4543 x + 17.373, R2 = 0.9949], ERBV1 rRT-PCR assay [ y = 3.4682 x + 11.719, R2 = 0.9997] and ERBV2 rRT-PCR assay [ y = 3.397 x + 26.055, R2 = 0.9959]).Back to article page