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

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

Short Description:

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.

Product Detail

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Product advantages

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.

Comply with the latest international cervical cancer screening strategy

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

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


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

Fluorescence PCR operation process

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

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.

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