COVID-19 TaqMan RT-PCR Detection Kit (N/ORF1ab genes) Dx
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Intended for in vitro diagnostics use.
This product is not available for purchase in Canada, or the United States.
COVID-19 TaqMan RT-PCR Detection Kit (N/ORF1ab genes) Dx
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Supporting Data
Figure 1: Multiplexed RT-PCR using the COVID-19 TaqMan RT-PCR Kit (N/ORF1ab genes) Kit for the specific detection of SARS-CoV-2 (N gene and ORF1ab) and an internal human control gene (RNase P). Shown are exemplary amplifcation curves following RT-PCR of 5 µL of the provided Positive Control (n = 3).
Figure 2: Highly sensitive and reproducible SARS-CoV-2 viral particle detection from varied sample matrices. Serial dilution of quantified heat-inactivated SARS-CoV-2 viral particles were spiked into preserved Nasal, Oral, and Saliva samples prior to RNA isolation using Norgen’s Saliva/Swab RNA Purification Kit (Cat. 69100) and RT-PCR to detect SARS-CoV-2 N gene and ORF1ab, and human RNase P (internal control). A) Linear detection of down to ten (10) viral copies per PCR reaction was reliably achieved in all sample types (n = 3; error is standard deviation).
Figure 3: Highly specific detection of SARS-CoV-2; No cross reactivity with other similar/major pathogens. Pathogen concentrations of ≥ 105 pfu/mL (for viruses), ≥ 106 CFU/mL (for bacteria), or 200,000 copies/uL of COVID-19 TaqMan RT-PCR Kit (N/ORF1ab genes) Positive Control were spiked into Nasal Swab and Saliva samples prior to RNA isolation using Norgen’s Saliva/Swab RNA Purification Kit (Cat. 69100) and RT-PCR to detect SARS-CoV-2 N gene and ORF1ab, and human RNase P (internal control). Positive SARS-CoV-2 detection was achieved only from SARS-CoV-2-spiked and Postive Control-spiked samples.
Figure 4: Robust detection, even with common sample contaminants. Nasal Swab and Saliva samples were supplemented with common contaminents either following or during collection, with a select subset shown here. 4 x LoD (40 viral copies per PCR reaction) of heat-inactivated SARS-CoV-2 viral particles were spiked into samples prior to RNA isolation using Norgen’s Saliva/Swab RNA Purification Kit (Cat. 69100) and RT-PCR to detect SARS-CoV-2 N gene and ORF1ab, and human RNase P (internal control). Positive SARS-CoV-2 detection was achieved in all cases (n = 5; error is standard deviation).
Figure 5: RT-PCR data interpretation key. In addition to this, the No Template Control (NTC) must not exhibit fluorescence above threshold; and each target in the N/ORF1ab/RP Positive Control must be detected (ideally <25 Ct). If these conditions are not met, the data is invalid, and the assay must be repeated.
Storage Conditions and Product Stability
- All kit components should be stored at -20°C upon arrival
- Repeated thawing and freezing (> 3x) of the Master Mix and Positive Control should be avoided, as this may affect the performance of the assay. If the reagents are to be used only intermittently, they should be frozen in aliquots.
- All reagents can be used until the expiration date specified on their labels.
Component | Cat. DxTM67300 (500 rxns) |
---|---|
N/ORF1ab/RP Primer & Probe Mix Dx | 850 μL |
N/ORF1ab/RP Positive Control Dx † | 500 μL |
2X One-Step RT-PCR Master Mix Dx | 7 x 1 mL |
Nuclease-Free Water (Negative control) | 2 x 1.25 mL |
Product Insert | 1 |
† Contains an in vitro RNA transcript for the three SARS-related target genes.