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Arylsulfatase A (ARSA) is a lysosomal enzyme that breaks down cerebroside 3-sulfate, a major component of myelin sheets, into cerebroside and sulfate. ARSA deficiency causes metachromatic leukodystrophy (MLD), a lysosomal storage disease of the central and peripheral nervous system with severe and progressive neurological symptoms. Recombinant human ARSA corresponds to the ARSA maturation peptide and has sulfatase activity.
Accession: AAH14210.2
Endotoxin < 1 EU/µg
Apparent Molecular Weight: 50-65 KDa, reducing conditions
Supplied as a 0.2 μm filtered solution of 20mM Tris-HCl, 300mM NaCl, pH 8.0.
The product is shipped on dry ice. Upon receipt, store it immediately at the temperature listed below.
| Form | Solution |
| Storage | Store at ≤ -70°C, stable for 6 months after receipt. |
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Products are for research use only. Not for human use. We do not sell to patients.
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