Seegene

Allplex HPV28 Detection

RM-03.007.050.001.002.001-0001-3
Human papillomavirus (HPV) / Genotyping / HPV genotyping, 28 individually identified types / Diagnostic real-time PCR kits

Allplex HPV28 Detection from Seegene is listed in Human papillomavirus (HPV): Genotyping: HPV genotyping, 28 individually identified types: Diagnostic real-time PCR kits.

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Pack sizes & catalog numbers

100 reactions · HP10372X

PRODUCT OVERVIEW

Product overview

Allplex HPV28 Detection supports genotype identification for HPV genotyping, 28 individually identified types. The manufacturer lists cervical specimen specimens. Ct reporting alone does not establish quantitative viral-load measurement. Follow the specified extraction, instrument and analysis workflow.

Browse molecular assays by targeted pathogen, then qualitative detection, quantitative measurement or genotyping. Multipathogen panels appear under each documented pathogen while retaining their complete panel identity.

For this workflow, compare the complete target panel, intended specimen, assay purpose, instrument, extraction workflow, controls, calibration and regional regulatory status. A Ct value alone does not establish quantitative performance, and species differentiation is not equivalent to within-pathogen genotyping. Use the specifications and official documentation below to assess this product against your protocol.

The indexed manufacturer catalog number is HP10372X.

Manufacturer
Seegene
Primary application group
Targeted molecular assays
Manufacturer catalog numbers
HP10372X
Evidence
Official manufacturer documentation; candidate compatibility requires protocol review
Target panel
HPV genotyping, 28 individually identified types
Assay readout
Genotyping
Intended use and workflow
CE-IVDR; verify regional availability
Format and compatibility
Allplex HPV28 Detection supports genotype identification for HPV genotyping, 28 individually identified types. The manufacturer lists cervical specimen specimens. Ct reporting alone does not establish quantitative viral-load measurement. Follow the specified extraction, instrument and analysis workflow.
Documented specimen types
Cervical specimen
Instrument and workflow requirements
Real-time PCR CFX96 Real-time PCR Detection System CFX96 DX System CFX Opus 96 Dx Automated Extraction SEEPREP32 Automated Extraction & PCR Setup Seegene STARlet Seegene STARlet-AIOS Seegene NIMBUS
Indexed pathogens
Human papillomavirus (HPV)
Assay purpose
Genotyping
Other specifications
Consult manufacturer documentation

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Your selection checklist

  • 01Exact target panel and qualitative or quantitative readout
  • 02Validated specimen, extraction method and calibration
  • 03Required instrument, software and reaction format
  • 04Diagnostic or research intended use and local availability

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Product sources and documentation

Allplex HPV28 Detection supports genotype identification for HPV genotyping, 28 individually identified types. The manufacturer lists cervical specimen specimens. Ct reporting alone does not establish quantitative viral-load measurement. Follow the specified extraction, instrument and analysis workflow.

Classification review: Allplex HPV28 Detection supports genotype identification for HPV genotyping, 28 individually identified types. The manufacturer lists cervical specimen specimens. Ct reporting alone does not establish quantitative viral-load measurement. Follow the specified extraction, instrument and analysis workflow. Manufacturer evidence

Official manufacturer product pageSeegene · Product details and documentation

Allplex HPV28 Detection supports genotype identification for HPV genotyping, 28 individually identified types. The manufacturer lists cervical specimen specimens. Ct reporting alone does not establish quantitative viral-load measurement. Follow the specified extraction, instrument and analysis workflow.

Seegene official product documentationOfficial manufacturer documentation; candidate compatibility requires protocol review · See original documentation for publication date

Primary classification is an editorial interpretation of the product name and cited source. Technical equivalence is not established by category membership. Read our methodology.