VARIANTnbs System

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Overview

The worldwide standard in automated newborn screening for sickle cell disease and other hemoglobin disorders; features fully automated high-capacity analysis of dried blood spot specimens
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Description

Description

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.

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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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250-3000
The Bio-Rad VARIANTnbs Sickle Cell Program offers a rapid 3-minute qualitative screen for the presence of hemoglobins F, A, S, D, C, and E in eluates of neonatal blood collected with one step sample preparation.

Documents

Documents

Number Description Options
B-213
VARIANT nbs Sickle Cell Program Brochure
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B-218
VARIANT nbs Operator Training Product Sheet
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