missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Iduronate 2 Sulfatase Polyclonal Antibody, Invitrogen™
Goat Polyclonal Antibody
Marca: Invitrogen PA519035
Detalles adicionales : Peso : 0.01000kg
Descripción
This antibody is tested in Peptide ELISA: antibody detection limit dilution 16,000.
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 | |
| Polyclonal | |
| 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 | |
| Goat | |
| Ammonium sulfate precipitation | |
| RUO | |
| 3423 | |
| -20° C, Avoid Freeze/Thaw Cycles | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 0.5 mg/mL | |
| TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3 | |
| P22304 | |
| Ids | |
| Synthetic peptide sequence (KHFRFRDLEEDP) corresponding to the internal amino acids of IDS | |
| 100 μg | |
| Primary | |
| Human | |
| Antibody | |
| IgG |