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NAGA Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech Non-distribution product as customer accommodation.

Rabbit Polyclonal Antibody

Manufacturer:  Proteintech Group IncSupplier Diversity Partner 150961AP

Catalog No. 50-172-9974

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NAGA (N-acetylgalactosaminidase, alpha), also known as alpha-galactosidase B or GALB, is a 411 lysosomal protein belonging to the glycosyl hydrolase 27 family that may exist as a homodimer and plays a critical role in glycolipid breakdown. NAGA encodes alpha-N-acetylgalactosaminidase, a lysosomal enzyme, which cleaves alpha-N-acetylgalactosaminyl groups from glycoconjugates. Mapping to human chromosome 22q13.2, NAGA defects are the cause of an autosomal recessive disorder with three phenotypes, known as Schindler disease (types I, II and III) or NAGA deficiency (types I, II and III). Characterized by neurologic manifestations that range in severity, Schindler disease type I is the most severe form, followed by type III, which may have mild-to-moderate effects. Schindler disease type II, also known as Kanzaki disease, is characterized by mild intellectual impairment and angiokeratoma corporis diffusum.


0.13 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
P17050, Q66H12, Q9QWR8
Alpha galactosidase B, D22S674, GALB, NAGA
150 μL
17939, 315165, 4668
Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
NAGA Fusion Protein Ag7172
Antigen Affinity Chromatography
Human, Mouse, Rat
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