Real-time PCR is one of the most well-known methods with good sensitivity and high accuracy for disease diagnostics. However, this technology used to have some disadvantages such as long turn-around-time or complicated workflow. Genesystem is proud to introduce SMARTCHEK® novel coronavirus (SARS-CoV-2) detection kit which is based on biochip sample format and provides relatively short turn-around-time with simple workflow while it offers key benefits of real-time PCR tests. The standard turn-around-time is 45 minutes using UF-300 real-time PCR platform of Genesystem. SMARTCHEK® novel coronavirus (SARS-CoV-2) detection kit has been developed to detect both N gene and RdRP gene of SARS-CoV-2. The primer pairs and probes for the detection of these two target genes are pre-labeled in the wells of the test chip so that user doesn't need to pipette primers and probes for running the test. Consult the experts of Genesystem for possible assay customization.

SMARTCHEK^® SARS-CoV-2 Fast Detection Kit has been developed to detect both RdRP gene and N gene of SARS-CoV-2, using GENECHECKER^® UF-300 and UF-340 Real-time PCR System. The primer pairs and probes are prelabeled in the test chip, and premix is preloaded in the reaction mixture tubes, which makes the workflow easy and simple.

This assay is containing COVID-19, Flu A&B, and RSV A&B specific primer pairs and can diagnose 5 main respiratory viruses infection in 40 minutes. This assay uses real-time polymerase chain reaction (PCR) technology and TaqMan^® Probe chemistry to detect target genes. Through PCR process, target-specific sequences are amplified, and target-specific primers and probes combine with a single strand of DNA and get amplified using DNA polymerase enzymes included in the premix formulation. Real-time amplification curves are displayed on the GENECHECKER^® UF-300 and UF-340 Real-time PCR System by the method of monitoring fluorescence signals generated from the reporter dye on 5’ end of the probes after exonuclease activities.

This assay is containing Mycobacterium tuberculosis specific primer pairs and can diagnose Mycobacterium tuberculosis infection in 40 minutes. This assay uses real-time polymerase chain reaction (PCR) technology and TaqMan^® Probe chemistry to detect target genes. Through PCR process, target-specific sequences are amplified, and target-specific primers and probes combine with a single strand of DNA and get amplified using DNA polymerase enzymes included in the premix formulation. Real-time amplification curves are displayed on the GENECHECKER^® UF-300 and UF-340 Real-time PCR System by the method of monitoring fluorescence signals generated from the reporter dye on 5’ end of the probes after exonuclease activities.

This assay is containing specific primer pairs of high risk HPV genes, such as Type 16, Type 18, High Risk HPV Group 1(16, 31, 33, 35, 52, and 58), High Risk HPV Group 2 (18, 39, 45, and 68), and High Risk HPV Group 3 (51, 56, and 59), and can diagnose Human papillomavirus infection in 40 minutes. This assay uses real-time polymerase chain reaction (PCR) technology and TaqMan® probe chemistry to detect target genes. The specific sequences of target genes are amplified through PCR process. Real-time amplification curves are displayed on GENECHECKER® UF-300 and UF-340 Real-time PCR System by the method of monitoring fluorescence signals generated from the reporter dye on 5’ end of the probes after exonuclease activities.

This assay is containing specific primer pairs and probes of Ureaplasma urealyticum (UU), Chlamydia trachomatis (CT), Mycoplasma hominis (MH), Mycoplasma genitalium (MG), Neisseria gonorrhoeae (NG), and Trichomanas vaginalis (TV) which are most common sexually transmitted pathogens. This assay uses real-time polymerase chain reaction (PCR) technology and TaqMan® probe chemistry to detect target pathogens. The specific sequences of target pathogen are amplified through PCR process. Real-time amplification curves are displayed on GENECHECKER® UF-300 and UF-340 Real-time PCR System by the method of monitoring fluorescence signals generated from the reporter dye on 5’ end of the probes after exonuclease activities.

Resistance to isoniazid is usually due to a mutation in katG or inhA and resistance to rifampin is usually due to a mutation in the rifampin resistance-determining region (RRDR) of the rpoB gene. This assay is containing specific primer pairs and probes of rpoB 1, 2, and 3 to detect RIF-resistant TB and katG, inhA to detect INH-resistant TB. This assay uses real-time polymerase chain reaction (PCR) technology and TaqMan^® probe chemistry to detect target genes. Real-time amplification curves are displayed on GENECHECKER^® UF-300 and UF-340 Real-time PCR System.