HPV DNA TEST Human papillomavirus nucleic acid detection kit(PCR-Fluorescence)

The test types completely cover the 18 HPV subtypes related to cervical cancer recommended by the CFDA for testing, namely: 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59 , 66, 68, 73, 82; and can separately accurately type HPV16 and 18 among them.

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Product Features

1. One tube reaction detects multiple HPV subtypes.

2. A variety of nucleic acid extraction programs to meet the needs of different samples.

3. Set up an internal reference system to exclude false-negative results.

4. Fluorescence PCR has high sensitivity and specificity.

5. High-throughput detection, 96 reactions per machine.

6. Quick response, running 1.5-2h each time.

7. Double channel detection to ensure the reliability of detection results.

8. Four-channel detection, suitable for four-channel fluorescent PCR machines (FAM, VIC, ROX, Cy5), such as: BIO-RAD, CFX96, ABI 7500

9. The classification of HPV16/18 can help improve sensitivity and control the referral rate of colposcopy;

10. HPV detection combined with cytological machine risk quantitative management can increase the detection rate of CIN3 and effectively control the number of colposcopy；

11. Unique Integrated Solution: with the company's liquid-based cytology products, one sampling and two detections can be realized, forming an integrated comprehensive detection program.

Instructions for Use

System preparation (10-30min)→sample extraction (30min)→sample addition (10-15mini)→PCR (1.5-2h)→result reading (10min).