VARIANT™nbs Newborn Hemoglobin Screening System

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Overview

VARIANT™ nbs Newborn Hemoglobin System

Using the VARIANT™ nbs System Is As Easy As 1-2-3

1. Import a Punch File.



2. Preview a Worklist.



3. Review results.

VARIANT™nbs Newborn Hemoglobin System

VARIANT™nbs Ensures Thorough Analysis for Hemoglobin Disorders

With the VARIANT™nbs Newborn Hemoglobin System, you get complete analysis for your newborn testing program. The  provides key benefits crucial for ensuring a thorough analysis for hemoglobin disorders:

  • Detects most clinically significant hemoglobin disorders
  • Detects the carrier status for abnormal hemoglobins
  • Detects many double heterozygote conditions

With the VARIANT™nbs you get the total picture the first time, allowing each baby to quickly receive the appropriate follow-up and care.

Example chromatogram showing a Hb E carrier with peaks presenting in both the Hb A and Hb E windows.

Example chromatogram showing a double heterozygote with peaks presenting in both the Hb S and Hb C windows.

The VARIANT™nbs 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 VARIANT™nbs 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 VARIANT™nbs provides the total hemoglobin picture.

The VARIANT™nbs 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 GDM Workstation
VARIANT™nbs GDM Workstation

250-3055
Workstation Computer that operates VARIANT™nbs System

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VARIANT™ Printer
VARIANT™ Printer

270-2385
Printer for use with VARIANT™nbs System

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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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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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