VARIANT™nbs Newborn Hemoglobin Screening System

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The VARIANTnbs is the established worldwide standard in automated newborn screening for sickle cell disease and other hemoglobin disorders. It features fully automated analysis and advanced result reporting for maximum efficiency. Using dried blood spot specimens, the VARIANTnbs identifies the most clinically significant hemoglobin variants, including hemoglobins F, S, A, C, D and E, as well as the carrier status for abnormal hemoglobin variants and many double-heterozygote conditions. The VARIANTnbs provides the total hemoglobin picture.

The VARIANTnbs is specifically designed for high-capacity screening and walk-away automation, reducing labor requirements and human error. Load up to three systems per workstation and up to 1,128 samples per run. Smart reports with optional pattern rules simplify data review while providing objective, accurate results. A flexible worklist import function eliminates file incompatibility issues. Reviewing and managing results is simple with electronic chromatogram storage and retrieval.

VARIANT™nbs Newborn Screening System

250-3010
Instrument for newborn screening of hemoglobins S, F, A, C, D, and E, includes bar code reader for sample tracking

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VARIANT™nbs Sickle Cell Program Reorder Pack

250-3000
Reagents, supplies for 1000 hemoglobin S, F, A, C, D, E tests of newborn dried blood using VARIANT™nbs System; aids detection of abnormal hemoglobin

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VARIANT™nbs Buffer 1

250-3001
2,500 mL bottle of additional buffer 1 used to run the VARIANT™nbs system

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Library of Variants
Library of Variants

400-4004
A reference compendium of over two hundred different hemoglobinopathy cases; for use with D-10™, VARIANT™, VARIANT™ II, and VARIANT™nbs systems.

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