Many countries in the world regulate the cultivation and trade with genetically modified organisms (GMO). The enforcement of such regulations depends on the ability to detect and quantify the presence of GMOs in food, feed, and seed products. The real-time qPCR method is sensitive and robust and is regarded as the gold standard for GMO analysis.
The Maize GMO 98140 qPCR Kit is designed for identifying GMO marker 98140 presence or absence in food, feed, and seed products using real-time quantitative polymerase chain reaction(qPCR), primers, and labeled probe. The Kit includes maize GMO 98140 Positive and Negative controls, PCR internal controls, qPCR SuperMix (M1), maize GMO 98140 Prime-Probe Mix(M2), in which the probe is labeled with Fam, and Hex is labeled for PCR internal control. These aids in the straightforward interpretation of the results.
KEY FEATURES1. DNA extraction: The methods for DNA extraction can be used for any suitable preparation of DNA purification from food samples. We recommend that the Fast genomic DNA extraction method be used for this purpose (catalog: TBS6008).
2. Set up a PCR reaction for each sample in 20 µL
| Reaction Component | Volume (µL) |
| qPCR Super Mix | 7.0 |
| Primer-probe Mix | 5.0 |
| Nuclease-free Water | 3.0 |
| DNA sample | 5.0 |
| Final Volume | 20 µL |
Internal control should be included as below: Positive Control or Negative control (5 µL /reaction).
3. Suggested PCR conditions
| Step | Amplification | PCR | |
| HOLD | CYCLE (40 cycles) | ||
| Denature | Anneal/ Extend | ||
| Temperature | 95 °C | 95 °C | 60 °C |
| Time | 1 min | 15 sec | 60 sec |
Additional information
| SIZE | 100 Reactions |
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TBS43001_Maize_GMO 98140_qPCR kit_V01_2022
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