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Invitrogen™ Arylsulfatase B Polyclonal Antibody

Description
This antibody is tested in Peptide ELISA: antibody detection limit dilution 64,000.
Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
Spécification
Spécification
| Antigène | Arylsulfatase B |
| Applications | Immunohistochemistry (Paraffin), Western Blot |
| Classification | Polyclonal |
| Concentration | 0.5 mg/mL |
| Conjugué | Unconjugated |
| Formule | TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3 |
| Expression | ARSB |
| Numéro d’ordre du gène | P15848 |
| Alias de gène | 1110007C02Rik; AI480648; Arsb; Arylsulfatase B; Arylsulfatase B (MPS VI); arylsulfatase B complex; arylsulfatase B regulation; arylsulfatase B structural; arylsulfatase B temporal regulation; As1; As-1; As-1r; As1-r; As-1s; As1-s; As-1t; As1-t; ASB; Asr-1; Ast-1; G4S; MPS6; N-acetylgalactosamine-4-sulfatase |
| Symboles de gène(s) | ARSB |
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