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cador N. caninum  PCR Reagent

For the identification of Neospora caninum DNA
  • A ready-to-use system for real-time PCR
  • Highly sensitive and specific identification of N. caninum DNA
  • Internal Control to monitor PCR inhibition
  • A full license for PCR without additional costs
The cador N. caninum PCR reagent is a highly sensitive and specific assay to identify Neospora caninum DNA in biological samples.

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Cat No./ID: 286115
cador N. caninum Reagent (96)
For 96 reactions: cador PCR + IC Reagents, cador N. caninum reagents
For Research Use Only. Not intended for any animal or human therapeutic or diagnostic procedures. No claim or representation is intended to provide information for the diagnosis, prevention or treatment of a disease. Regulatory requirements vary by country, product may not be available in your geographic area.

Efficient and precise identification of N. caninum DNA over a wide linear range.
Duplex real-time PCR was carried out using the cador N. caninum PCR Reagent and the Rotor-Gene Q according to the supplied protocol. N. caninum DNA was serially diluted as indicated in the figure. Each concentration was analyzed in triplicate. [A] Amplification plots for N. caninum DNA (one replicate is shown for each template dilution). [B] Amplification plots for IC DNA (one replicate is shown for each template dilution). [C] The log template amount was plotted versus mean CT value, demonstrating a high efficiency, linearity, and precision in identification of N. caninum DNA. Error bars represent ± 1 SD of 3 replicates.
The cador N. caninum Reagent contains reagents and enzymes for the specific and efficient amplification of highly conserved regions of the N. caninum genome. Inhibition and other malfunctions of PCR are determined by measuring the fluorescence signal in the yellow channel via amplification of the Internal Control (IC), which does not influence the amplification of the analytical PCR for N. caninum. An external positive control (N. caninum Control DNA, containing the targeted N. caninum DNA) is also supplied. N. caninum DNA is detected efficiently and precisely over a wide linear range (see the figure Efficient and precise identification of N. caninum DNA over a wide linear range).
Pathogen identification by the polymerase chain reaction (PCR) is based on the amplification of specific regions of the pathogen genome. In real-time PCR, the amplified product is detected using fluorescent dyes. These are usually linked to oligonucleotide probes that bind specifically to the amplified product. Monitoring the fluorescence intensities during the PCR run (i.e., in real time) allows detection of the accumulating product without having to re-open the reaction tubes afterward, which reduces the risk of cross contamination.
The cador N. caninum PCR Reagent contains a primer-probe set specific for a highly conserved region of the N. caninum genome. The reagent also includes a heterologous amplification system as an internal control to ensure the correct interpretation of negative results, and an external positive control. Real-time PCR detection is carried out on a real-time PCR cycler, such as the Rotor-Gene Q.
Bacterial DNA can be manually isolated from samples using the QIAamp cador Pathogen Mini Kit. The isolated DNA is ready for use in real-time PCR with the cador N. caninum PCR Reagent on a real-time PCR cycler, such as the Rotor-Gene Q.
The cador N. caninum PCR Reagent is designed to identify Neospora caninum DNA in biological samples using polymerase chain reaction (PCR).

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