Skip to main content
Fig. 1 | BMC Veterinary Research

Fig. 1

From: Development of TaqMan-based real-time RT-PCR assay based on N gene for the quantitative detection of feline morbillivirus

Fig. 1

a The detection limit of qRT-PCR assay based on cRNA copy number. Amplification plot of 10-fold serial diluted cRNA ranging from 1.74 × 1011 to 1.74 × 104 copies/μL. b Standard curve of qRT-PCR assay. Ten-fold dilutions of control cRNA were assessed with the qRT-PCR assay. Log copies per μL and quantitation cycle (Cq) are plotted on the x-axis and y-axis, respectively

Back to article page

BMC Veterinary Research

ISSN: 1746-6148

Contact us