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Alglucosidase alfa

Alglucosidase alfa (rhGAA) is a hydrolytic lysosomal glycogen-specific recombinant human α-glucosidase. Alglucosidase alfa can be used for Pompe disease research[1].

Product Specifications

CAS Number

420784-05-0

Product Name Alternative

RhGAA

UNSPSC

12352204

Target

Glycosidase

Related Pathways

Metabolic Enzyme/Protease

Field of Research

Metabolic Disease

Solubility

10 mM in DMSO

Smiles

[Alglucosidasealfa]

References & Citations

[1]Dornelles AD, et al. Efficacy and safety of enzyme replacement therapy with alglucosidase alfa for the treatment of patients with infantile-onset Pompe disease: a systematic review and metanalysis. Front Pediatr. 2024 Feb 15;12:1310317.

Shipping Conditions

Room temperature

Scientific Category

Inhibitory Antibodies

Clinical Information

Launched

Frequently Asked Questions

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