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Iduronate 2 Sulfatase Monoclonal Antibody (OTI4G2), Invitrogen™
Mouse Monoclonal Antibody
Marca: Invitrogen MA525866
Detalles adicionales : Peso : 0.01000kg
Descripción
Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. Iduronate-2-sulfatase has a strong sequence similarity with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described.Especificaciones
| Iduronate 2 Sulfatase | |
| Monoclonal | |
| 1 mg/mL | |
| PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| P22304, Q08890 | |
| Ids | |
| Full length human recombinant protein of IDS produced in HEK293T cell | |
| 100μL | |
| Primary | |
| Canine, Human, Mouse, Non-human Primate, Rat | |
| Antibody | |
| IgG2a |
| Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot | |
| OTI4G2 | |
| Unconjugated | |
| Ids | |
| alpha-L-iduronate sulfate sulfatase; AW214631; Ids; Iduronate 2-sulfatase; iduronate 2-sulfatase (Hunter syndrome); iduronate 2-sulfatase 14 kDa chain; Iduronate 2-sulfatase 42 kDa chain; iduronate sulfatase; iduronate-2-sulfatase; idursulfase; MPS2; SIDS | |
| Mouse | |
| Affinity Chromatography | |
| RUO | |
| 15931, 3423, 363513, 492194 | |
| -20° C, Avoid Freeze/Thaw Cycles | |
| Liquid |