CANDIDATE SUBSTITUTION GROUP

Diagnostic real-time PCR kits

RM-C-03.007.038.001.001.001

Compare qualitative molecular assays for Haemophilus ducreyi that detect the presence of pathogen nucleic acid, including documented species or type differentiation. Target coverage: CMV, HSV-1, HSV-2, VZV, H. ducreyi, C. trachomatis LGV and T. pallidum panel. Assay format: Diagnostic real-time PCR kits.

1 products1 manufacturersFinal category

About Diagnostic real-time PCR kits

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.

Match the exact pathogen panel, qualitative or quantitative readout, specimen type, extraction method and instrument protocol. Diagnostic and research-use versions are separate products. Related assays may overlap in targets without providing the same result or a validated replacement workflow.

When selecting products, 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.

Products in this final group are candidates for comparison. Check the individual specifications and manufacturer protocols before substituting one product for another.

Products in this category

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Research readiness

Candidate classification still requires protocol validation.

Seegene

Allplex Genital ulcer Assay

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Herpes simplex virus 1 (HSV-1) / Qualitative / CMV, HSV-1, HSV-2, VZV, H. ducreyi, C. trachomatis LGV and T. pallidum panel / Diagnostic real-time PCR kits

Allplex Genital ulcer Assay supports qualitative detection and target identification for CMV, HSV-1, HSV-2, VZV, H. ducreyi, C. trachomatis LGV and T. pallidum panel. The manufacturer lists genital swab urine liquid-based cytology (e.g., thinprep and surepath) specimens. Ct reporting alone does not establish quantitative viral-load measurement. Follow the specified extraction, instrument and analysis workflow.

RM-03.007.044.001.002.001-0001-2SD9802X1 pack optionManufacturer link
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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

ALTERNATIVE DOES NOT MEAN IDENTICAL

What to check before choosing a product

Final groups are designed around experimental substitution requirements. Group membership is provisional until the necessary technical details have been verified for the intended experiment.

Start with your application, then verify the technical requirements against each manufacturer’s documentation.

Only one manufacturer is currently indexed in this category. Cross-manufacturer coverage is still incomplete.

Latest manufacturer research

Reviewed 2026-11-07. 1 additional product indexed in this pass.

Manufacturer evidence reviewed for pathogen coverage, readout, target differentiation, intended use and workflow. Overlapping panels appear under each supported pathogen while exact-panel groups remain separate.

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Broader catalog resources for this branch. These links are discovery starting points, not verified replacements for individual products.