Laboratory Equipment

Galactosemia is an inherited metabolic abnormality comprising three distinctive clinical entities of the galactose pathway defects. Classic galactosemia is due to -Dgalactose- 1-phosphate-uridyl-transferase (GALT) defect (1). The test principle is based on extraction of Galactose & Galactose-1-phosphate from dried blood spot followed by enzymatic conversion of Galactose-1-phosphate & Galactose. Two kinds of extraction methods (acidic and heat) can be used for extraction step.

1.Compact Design

2. Quantitative UPLC – MS/MS applications

3. Rapid, reliable and reproducible quantitative data for the clinical laboratory

4. Clinical laborataries have access to the selectively, sensitivity and versatility of LC-MS

5. Reduces complexity and maximizes throughput and uptime

6. The system is controlled by Mass Lynx IVD Software