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MSUD

Biorex Diagnostics manufactures, develops and supplies an extensive range of high quality neonatal screening tests for the detection of inborn errors of metabolism.

Maple syrup urine disease (MSUD) is an inborn error of metabolism detectable by neonatal screening. Deficiency of the branched-chain 2-keto acid dehydrogenase leads to the accumulation of branched-chain amino acids (BCAA) leucine, valine, isoleucine, and alloisoleucine.

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Description

Product Name CAT.No Details
MSUD BXC0811A 50T

 

 

Product Description

The Biorex Diagnostics Maple Syrup Urine Disease (MSUD) Test is a high-quality neonatal screening assay designed for the early detection of MSUD, a rare but potentially life-threatening inborn error of metabolism. Simple, reliable, and highly sensitive, this test is ideal for clinical laboratories, hospitals, and newborn screening programmes to support timely diagnosis and intervention.

Key Features
• Neonatal-focused – compatible with dried blood spots, plasma, or serum for minimally invasive sampling
• Accurate quantification – measures leucine, isoleucine, valine, and alloisoleucine with precision
• Rapid and reliable results – enables timely clinical decisions and early dietary intervention
• High sensitivity and specificity – detects even mild elevations for early identification
• User-friendly – straightforward procedures suitable for high-throughput neonatal screening
• Laboratory integration – compatible with standard platforms and LIMS
• Cost-effective – tailored for large-scale newborn screening programmes

The Biorex Diagnostics MSUD Test provides a trusted, efficient, and clinically relevant solution for neonatal screening and early diagnosis of Maple Syrup Urine Disease. Its combination of accuracy, reliability, and simplicity supports early intervention, optimised workflow, and improved long-term health outcomes for affected infants.

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Storage

2-8°C