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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. ABIN1590057
Reactivity Human, Mouse, Pig, Rat
Clonality Polyclonal
Application ELISA, IF, WB
Quantity 100 μg
Cat. No. ABIN969053
Reactivity Human
Clonality Monoclonal
Application ELISA, WB
Quantity 100 μL
Cat. No. ABIN3022135
Reactivity Human, Mouse, Rat
Clonality Polyclonal
Application IHC, WB
Quantity 100 μL
Cat. No. ABIN2854962
Reactivity Human, Rat
Clonality Polyclonal
Application IP, IHC (p), WB
Quantity 100 μL
Cat. No. ABIN2854995
Reactivity Human
Clonality Polyclonal
Application ICC, IF, IHC (p), WB
Quantity 100 μL
Cat. No. ABIN5611242
Reactivity Human
Clonality Monoclonal
Application ELISA, FACS, IHC, WB
Quantity 0.1 mg
Cat. No. ABIN350194
Reactivity Human, Mouse, Rat
Clonality Polyclonal
Application IHC, WB
Quantity 100 μL
Cat. No. ABIN3020412
Reactivity Human
Clonality Polyclonal
Application IF, IHC
Quantity 100 μL
Cat. No. ABIN6391378
Reactivity Human, Mouse
Clonality Polyclonal
Application ELISA, FACS, IF, IHC, WB
Quantity 100 μg
Cat. No. ABIN2856652
Reactivity Human
Clonality Polyclonal
Application ICC, IF, IHC (p), WB
Quantity 100 μL
Cat. No. ABIN5539604
Reactivity Human
Clonality Polyclonal
Application ELISA, IF
Quantity 100 μg

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