Fabry Disease
Fabry disease (also known as alpha-galactosidase-A deficiency) is an inherited lysosomal storage disease that is caused by the lack of or faulty enzyme needed to metabolize lipids and fat-like substances. Research on Fabry Disease has focused on the targets listed below.
Important Targets related to Fabry Disease
The following targets are directly related to research on Fabry Disease. Find Antibodies, Kits, Reagents and other products.
Featured Antibodies for Fabry Disease Research
Product
Cat. No.
Reactivity
Clonality
Application
Quantity
Datasheet
Cat. No.
ABIN5539604
Reactivity
Human
Clonality
Polyclonal
Application
ELISA, IF
Quantity
100 μg
Datasheet
Datasheet
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