Kodia Biotechnology Inc

Kodia Biotechnology Inc

Henan,China

Kodia Biotechnology Inc

Henan,China

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Kodia Biotechnology Inc
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Kodia Biotechnology Inc

Henan,China

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Human Papillomavirus (HPV) E6/E7 mRNA Detection Kit (Branched DNA signal amplification method)

FOB Price : Get a Price/Quote

Min.Order : 92 Piece(s)

Certification : CFDA,CE

Brand Name : Kodia

Payment Terms : L/C,T/T,D/P

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product information

  • brand name : Kodia

  • certification : CFDA,CE

  • min.order : 92 Piece(s)

  • warranty : /

  • payment terms : L/C,T/T,D/P

  • Packaging : /

  • Specification : /

  • place of origin : unknown

product description

The first cervical cancer risk assessment kit in China that has been clinically and pathologically verified to detect viral E6/E7 mRNA.
The HPV E6/E7 mRNA detection kit detects 14 high-risk HPV E6/E7 mRNAs announced by the World Health Organization. It has higher clinical specificity than similar products. It is the only domestic cervical cancer screening product used to "Assess the Risk of Cervical Lesions"., is the primary screening method recommended by cervical cancer screening guidelines.

● Detection target: The 14 high-risk human papillomavirus (HPV) oncogene E6/E7 mRNAs that cause cervical cancer announced by WHO: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68 type
● Detection demographic: Cervical cancer screening and physical examination group, Outpatient population, individuals with cervical abnormalities, Follow-ups after cervical lesions surgery
● Test samples: Cervical exfoliated cell sample
● Conducted clinical effectiveness verification trials and had clear clinical indications

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Human Papillomavirus (HPV) E6/E7 mRNA Detection Kit (Branched DNA signal amplification method)
share :

product information

product description

The first cervical cancer risk assessment kit in China that has been clinically and pathologically verified to detect viral E6/E7 mRNA.
The HPV E6/E7 mRNA detection kit detects 14 high-risk HPV E6/E7 mRNAs announced by the World Health Organization. It has higher clinical specificity than similar products. It is the only domestic cervical cancer screening product used to "Assess the Risk of Cervical Lesions"., is the primary screening method recommended by cervical cancer screening guidelines.

● Detection target: The 14 high-risk human papillomavirus (HPV) oncogene E6/E7 mRNAs that cause cervical cancer announced by WHO: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68 type
● Detection demographic: Cervical cancer screening and physical examination group, Outpatient population, individuals with cervical abnormalities, Follow-ups after cervical lesions surgery
● Test samples: Cervical exfoliated cell sample
● Conducted clinical effectiveness verification trials and had clear clinical indications

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