Triplex Fluorescent RT-PCR Test Kit for Foot-and-Mouth Disease Virus Type SAT1, Foot-and-Mouth Disease Virus and Foot-and-Mouth Disease Virus Type O
Triplex Fluorescent RT-PCR Test Kit for Foot-and-Mouth Disease Virus Type SAT1, Foot-and-Mouth Disease Virus and Foot-and-Mouth Disease Virus Type O
Simultaneously detects Foot-and-Mouth Disease Virus serotype SAT1 (FAM), Foot-and-Mouth Disease Virus (HEX), and Foot-and-Mouth Disease Virus serotype O (ROX); high sensitivity, strong specificity, and excellent reproducibility; available in liquid and lyophilized formulations.
Specification
Specification
Precautions
Precautions
Intended use: For the detection of nucleic acids of Foot-and-Mouth Disease Virus serotype SAT1, Foot-and-Mouth Disease Virus, and Foot-and-Mouth Disease Virus serotype O in samples from cloven-hoofed animals such as pigs, cattle, and sheep, including vesicular epithelium, vesicular fluid, serum, OP fluid, lymph nodes, and tonsil tissues.
Storage
Storage
Validity Period
Validity Period

Triplex Fluorescent RT-PCR Test Kit for Foot-and-Mouth Disease Virus Type SAT1, Foot-and-Mouth Disease Virus and Foot-and-Mouth Disease Virus Type O
Intended use: For the detection of nucleic acids of Foot-and-Mouth Disease Virus serotype SAT1, Foot-and-Mouth Disease Virus, and Foot-and-Mouth Disease Virus serotype O in samples from cloven-hoofed animals such as pigs, cattle, and sheep, including vesicular epithelium, vesicular fluid, serum, OP fluid, lymph nodes, and tonsil tissues.
Application scenarios: Suitable for abnormal screening, introduction quarantine monitoring, and breeding livestock transportation.
Experimental data (image): In clinical sample validation, the detection rate for all inactivated positive samples was 100%. The detection rates for both sensitivity quality control samples and weak positive clinical samples were higher than those of the standard method, indicating that this kit has excellent sensitivity.
Test results of three batches of kits compared with the WOAH reference method:

Test results of three batches of kits compared with the national standard method:


