Product Overview
本产品基于经典且经济的常规RT-PCR技术开发,通过特异性引物对番茄环斑病毒(ToRSV)进行扩增,配合琼脂糖凝胶电泳(扩增产物449 bp)即可直观判定结果。适合具备基础分子生物学操作条件的实验室进行常规初筛与检疫鉴定。
Core Advantages
经典标准:符合 SN/T 2670-2010 出入境检验检疫行业标准。
成本效益高:无需昂贵的荧光定量PCR设备即可完成精准定性检测。
结果直观:电泳条带清晰,结果判定标准明确。

Enzymatic reaction based on DNA polymerase that uses real-time fluorescence monitoring of PCR amplification to achieve qualitative or quantitative detection of target nucleic acids.
Extract target DNA/RNA from samples and remove inhibitors such as proteins and polysaccharides to obtain high-purity nucleic acid templates for PCR.
Under the guidance of specific primers and fluorescent probes, DNA polymerase catalyzes dNTP incorporation to synthesize a new strand, releasing one fluorescent signal per amplification cycle.
The instrument acquires fluorescence signals in real time and performs precise quantification of target nucleic acids by comparing Ct values against a standard curve.
Rigorous quality control system ensures stability and reliability for every product batch.
Optimized reaction conditions to achieve the best balance between amplification efficiency and specificity.
| Steps | 温度 | Time | Cyclic Number | Description |
|---|---|---|---|---|
| pre-deformation | 95°C | 3-5 min | 1 | Activate DNA polymerase |
| 变性 | 95°C | 10-15 sec | 40-45 | Collect fluorescence signal |
| Annealing/Extension | 55-60°C | 30-40 sec |
Note: Specific reaction conditions may vary depending on the instrument model and target analyte. Please refer to the product manual or consult a technical expert.
Widely compatible with mainstream real-time PCR instruments to meet diverse laboratory equipment needs
本产品基于经典且经济的常规RT-PCR技术开发,通过特异性引物对番茄环斑病毒(ToRSV)进行扩增,配合琼脂糖凝胶电泳(扩增产物449 bp)即可直观判定结果。适合具备基础分子生物学操作条件的实验室进行常规初筛与检疫鉴定。
结果直观:电泳条带清晰,结果判定标准明确。
A professional technical team providing comprehensive product application and testing solution support.
Our technical expert team will provide you with professional product consulting and customized solutions.
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