
Estradiol G2 Elecsys 100T | REF 3000079190
Roche Elecsys Estradiol G2 immunoassay reagent kit, 100 tests, REF 3000079190, for use on compatible Roche cobas immunoassay analyzers.

The Roche Anti-HCV Elecsys reagent (REF 3290352190) is an electrochemiluminescence immunoassay (ECLIA) designed for the qualitative determination of antibodies to the hepatitis C virus (anti-HCV) in human serum and plasma. It is intended for use on Roche cobas e immunoassay analyzers as part of routine infectious disease screening workflows in clinical laboratories.
Key Features
- Assay technology: Electrochemiluminescence immunoassay (ECLIA) based on a double-antigen sandwich principle using recombinant HCV antigens (core, NS3, NS4).
- Sample material: Human serum and plasma (refer to IFU for accepted anticoagulants).
- Platform compatibility: Roche cobas e immunoassay analyzers (refer to Roche product matrix for exact module compatibility).
- Ready-to-use reagent pack with onboard stability as defined in the official Method Sheet.
- Result type: Qualitative (reactive / non-reactive) based on a cutoff index.
- Traceability: Barcoded reagent cassette for automated handling and lot tracking.
Clinical Applications
- Laboratory screening for antibodies to hepatitis C virus as an aid in the diagnosis of HCV infection.
- Support for infectious disease testing panels in hospital, reference and clinical laboratories.
- Suitable for high-throughput immunoassay workflows on compatible Roche cobas e systems.
- Intended use, indications and regulatory status: Not specified in the located sources; refer to the official Roche Instructions for Use (IFU) and local regulatory labeling.
Product Information
- Product name: Anti-HCV Elecsys
- Brand: Roche
- Category: Roche Reagents
- REF / UPN: 3290352190
- Kit size / number of tests: Not specified in the located sources
- Storage conditions: Not specified in the located sources; refer to the official Method Sheet / IFU
- Shelf life and onboard stability: Not specified in the located sources; refer to the official Method Sheet / IFU
- Regulatory status: Not specified in the located sources
Tell us what product you need and share a few details.
We connect your request with the most relevant verified brands.
Relevant supplier options can respond with availability, documentation context, and quote details.
Practical answers for procurement teams reviewing this product page.
Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.
Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.
Related products are connected through structured catalog data such as brand, category, product family and country assignment.
No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.
Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.
Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.
Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.
The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.