Employs one-step Reverse Transcription PCR (RT-PCR) to amplify extracted viral RNA in a single tube. Incorporates CLP™ (Customized Linker Primer) technology, which controls non-specific priming and optimizes Tm conditions to maximize specificity and sensitivity. Provided in a Maxime™ dried premix format to enhance pipetting precision, and contains 8-MOP to prevent post-PCR carry-over contamination. Results are visualized by agarose gel electrophoresis.

Utilizes one-step RT-PCR combining reverse transcription of viral genomic RNA into cDNA with subsequent PCR amplification in a single reaction. Employs CLP™ technology to prevent non-specific band formation and Maxime™ dry-lyophilized master mix pre-dispensed in strip tubes. This eliminates manual master mix aliquoting steps, minimizing contamination risk and error. Target bands are verified via standard gel electrophoresis.

Employs probe-based Real-time Reverse Transcription PCR. RNA extracted from specimens is converted into cDNA and amplified using primers specific to the highly conserved M gene. Fluorescent TaqMan probes target this sequence in real-time, emitting fluorescence detected by the qPCR optical module during the cycle. Incorporates high-performance RTase and Hot Start DNA polymerase in a stabilized premix to maximize sensitivity and avoid false positives.

Combines reverse transcription and real-time PCR amplification in a single tube using TaqMan probe-based chemistry. Focuses on the H5-specific sequence of the Hemagglutinin gene. The fluorescent probe, upon binding to the amplified target cDNA, is cleaved by the 5' nuclease activity of the DNA polymerase, generating real-time fluorescence signals. Includes internal positive controls (IPC) to verify reaction efficiency and safeguard clinical quarantine diagnostics.

Developed in coordination with the Animal and Plant Quarantine Agency (APQA) for standardized genetic testing. Operates on real-time probe-based RT-PCR. Targeting the specific H7 hemagglutinin sequence, it monitors cDNA synthesis and exponential DNA amplification using sequence-specific primers and fluorophore-quenched probes, ensuring unmatched typing precision and high analytical sensitivity.

Utilizes probe-based real-time PCR targeting the highly conserved regions of the IBV viral genome. The one-step RT-PCR reaction combines reverse transcriptase and Hot Start PCR polymerase to convert single-stranded RNA into cDNA and amplify it. Incorporates CLP™ technology to prevent primer-dimer formation and non-specific priming. A dual-channel optical profile detects the target pathogen and an Internal Positive Control (IPC) to prevent false-negative interpretation.

Designed as a probe-based one-step real-time RT-PCR. Targets NDV genomic RNA, performing cDNA synthesis and amplification simultaneously in a stabilized master mix. Utilizes 5' nuclease TaqMan probe chemistry to isolate the NDV signal in the primary channel while monitoring amplification validation in the HEX/VIC channel via a pre-mixed internal control (IPC), ensuring robust diagnostics in diagnostic labs.