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Procleix Ultrio Elite Assay (FDA Approved and CE Marked)
Ref. GRF-PROCLEIX-ULTRIO-ELITE-ASSAYSingle-tube, highly sensitive detection of HIV-1 RNA, HIV-2 RNA, HCV RNA, and HBV DNA in blood and plasma donations.
Tests per card
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Packaging
1000 or 5000 tests
Contact us for product availability and technical details.
About the Product
Single-tube, highly sensitive detection of HIV-1 RNA, HIV-2 RNA, HCV RNA, and HBV DNA in blood and plasma donations.
The Procleix Ultrio Elite assay is CE marked and FDA approved.
Technical Characteristics
| Regulatory status | FDA Approved and CE Marked |
|---|---|
| Assay chemistry | Qualitative, transcription-mediated amplification (TMA) |
| Indication | Blood screening, source plasma, cadaveric (non-heart-beating) donors |
| Collection tube | Serum or plasma collected in K2EDTA, K3EDTA, Greiner K2EDTA sep collection tubes, or BD PPT tubes |
| Pool sizes | IDT-NAT, 4, 8, 16, 96 |
| Detected virus | HIV-1 group M (subtypes A-H, K, CRF01_AE, CRF03_AB), N, O; HIV-2 subtypes A, B; HCV genotypes 1-6 (subtypes 1a, 1b, 2a/c, 2b, 3a, 3b, 3e, 4a, 4b/c, 5a, 6a); HBV genotypes A-H |
Technical Information
No technical information available for this product.
Compatibility
Platform: Procleix Panther system
Packaging
1000 or 5000 tests