Arylsulfatase A (ARSA)

MLD; ASA; Metachromatic Leucodystrophy; Cerebroside-sulfatase
Arylsulfatase A (ARSA)
Arylsulfatase A hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene
The predicted amino acid sequence comprised 507 residues, including a putative signal peptide of 18 residues. The sequence contains 3 potential N-glycosylation sites. The cDNA hybridized to 2.0- and 3.9-kb species in RNA from human fibroblasts and human liver.
Organism species: Homo sapiens (Human)
Organism species: Mus musculus (Mouse)
  • Protein RPG619Mu01Recombinant Arylsulfatase A (ARSA)Customize
  • AntibodyPAG619Mu01Polyclonal Antibody to Arylsulfatase A (ARSA)Customize
  • AntibodyMAG619Mu21Monoclonal Antibody to Arylsulfatase A (ARSA)Customize
  • Assay KitSEG619MuELISA Kit for Arylsulfatase A (ARSA)Customize
  • Assay KitSCG619MuCLIA Kit for Arylsulfatase A (ARSA)Customize
Organism species: Rattus norvegicus (Rat)
  • Protein RPG619Ra01Recombinant Arylsulfatase A (ARSA)Customize
  • AntibodyPAG619Ra01Polyclonal Antibody to Arylsulfatase A (ARSA)Customize
  • AntibodyMAG619Ra21Monoclonal Antibody to Arylsulfatase A (ARSA)Customize
  • Assay KitSEG619RaELISA Kit for Arylsulfatase A (ARSA)Customize
  • Assay KitSCG619RaCLIA Kit for Arylsulfatase A (ARSA)Customize
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