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SGSH Protein, Human, Recombinant (His)

(Synonyms: Sulphamidase, Sulfoglucosamine Sulfamidase, SGSH, N-Sulphoglucosamine Sulphohydrolase, HSS) Copy Product Info

Synonyms: Sulphamidase, Sulfoglucosamine Sulfamidase, SGSH, N-Sulphoglucosamine Sulphohydrolase, HSS

Catalog No. TMPJ-01002 Copy Product Info
N-Sulphoglucosamine Sulphohydrolase (SGSH) is an important member of the sulfatase family which is involved in the degradation of heparin sulfate. SGSH binds one calcium ion per subunit as a cofactor. SGSH catalyzes N-sulfo-D-glucosamine and H2O to D-glucosamine and sulfate. SGSH deficiency is result in mucopolysaccharidosis type 3A (MPS3A), a recessive lysosomal storage disease characterized by neurological dysfunction but relatively mild somatic manifestations.
SGSH Protein, Human, Recombinant (His)
Pack SizePriceUSA StockGlobal StockQuantity
10 µg$18335 days35 days
20 µg$29235 days35 days
50 µg$54535 days35 days
100 µg$79235 days35 days
200 µg$1,15035 days35 days
500 µg$1,90035 days35 days
1 mg$2,73035 days35 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Bioactivity
Activity has not been tested. It is theoretically active, but we cannot guarantee it. If you require protein activity, we recommend choosing the eukaryotic expression version first.
Description
N-Sulphoglucosamine Sulphohydrolase (SGSH) is an important member of the sulfatase family which is involved in the degradation of heparin sulfate. SGSH binds one calcium ion per subunit as a cofactor. SGSH catalyzes N-sulfo-D-glucosamine and H2O to D-glucosamine and sulfate. SGSH deficiency is result in mucopolysaccharidosis type 3A (MPS3A), a recessive lysosomal storage disease characterized by neurological dysfunction but relatively mild somatic manifestations.
Species
Human
Expression System
HEK293 Cells
TagC-6xHis
Accession NumberP51688
Amino AcidArg21-Leu502
ConstructionArg21-Leu502
Protein Purity
Greater than 95% as determined by reducing SDS-PAGE. (QC verified)
Endotoxin< 0.1 ng/µg (1 EU/µg) as determined by LAL test.
FormulationSupplied as a 0.2 μm filtered solution of 20 mM Tris-HCl, 150 mM NaCl, 1 mM CaCl<sub>2</sub>, 10% Glycerol, pH 7.5.
SynonymsSulphamidase, Sulfoglucosamine Sulfamidase, SGSH, N-Sulphoglucosamine Sulphohydrolase, HSS
Research Background
N-Sulphoglucosamine Sulphohydrolase (SGSH) is an important member of the sulfatase family which is involved in the degradation of heparin sulfate. SGSH binds one calcium ion per subunit as a cofactor. SGSH catalyzes N-sulfo-D-glucosamine and H2O to D-glucosamine and sulfate. SGSH deficiency is result in mucopolysaccharidosis type 3A (MPS3A), a recessive lysosomal storage disease characterized by neurological dysfunction but relatively mild somatic manifestations.
Chemical Properties
Molecular Weight63 KDa (reducing condition)
Storage & Solubility Information
ShippingProteins are shipped with blue ice.
StorageLyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.

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Related Tags: SGSH Protein, Human, Recombinant (His) chemical structure | SGSH Protein, Human, Recombinant (His) molecular weight