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Iduronate 2 Sulfatase Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Marca: Invitrogen PA5121834
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 | |
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 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
3423 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
0.5 mg/mL | |
PBS with 50% glycerol and 0.05% ProClin 300 | |
P22304 | |
Ids | |
Recombinant protein Iduronate-2-Sulfatase. The antigen corresponds to amino acid range 95-289 of the target protein. | |
20 μL | |
Primary | |
Human | |
Antibody | |
IgG |