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| Cat.No | ACP04802 | Target Name | GALNS |
|---|---|---|---|
| Target Synonyms | GALNSN-acetylgalactosamine-6-sulfatase; EC 3.1.6.4; Chondroitinsulfatase; Chondroitinase; Galactose-6-sulfate sulfatase; GalN6S; N-acetylgalactosamine-6-sulfate sulfatase; GalNAc6S sulfatase | Form | Liquid or Lyophilized powder |
| Expression System | Yeast | Expression Range | 27-522aa |
| Mol Weight | 57.4kDa | Protein Length | Full Length of Mature Protein |
| Purity | Greater than 90% as determined by SDS-PAGE. | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | P34059 |
|---|
Uniprot Id
P34059
Target Species
Human
Target Name
GALNS
Target Full Name
N-acetylgalactosamine-6-sulfatase
Target Involvement
Mucopolysaccharidosis 4A (MPS4A)
Target Subcellular Location
Lysosome.
Target Protein Families
Sulfatase family
Target Research Area
Signal Transduction
Target Synonyms
GALNSN-acetylgalactosamine-6-sulfatase; EC 3.1.6.4; Chondroitinsulfatase; Chondroitinase; Galactose-6-sulfate sulfatase; GalN6S; N-acetylgalactosamine-6-sulfate sulfatase; GalNAc6S sulfatase
Target Background
This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder.
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