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■Product description

HPV infection is closely related to the development of cervical cancer, and the second edition of ``Cervical Cancer Prevention: Guidelines for Screening and Treatment of Cervical Premalignant Lesions'' published by WHO in 2021. , recommends HPV DNA testing as the preferred method of cervical cancer screening. As indoor quality control for HPV nucleic acid testing -Each batch must contain at least one negative and one positive control. -Positive controls must include one or more common HPV high-risk types. (For example: HPV16, 18, 52, 58, etc.) - Both negative and positive controls should be involved in the detection process from extraction to amplification.

■Product features

・Derived from cell lines that are close to actual clinical samples and involved in the entire assay process from extraction to amplification ・Proprietary third-party standard products, compatible with common clinical testing platforms and methodologies ・Liquid standard product, no need for re-melting; stable performance and reliable quality ・Provide positive standard products at high, medium, and low concentration levels and simultaneously meet various customer needs ・Genome copy number has been accurately quantified by digital PCR

■Product application

Compatible with common clinical detection technology platforms such as fluorescence quantitative PCR, hybridization capture, and microfluidics

  • Product

    HPV standard solution

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