GNS Protein (His tag)

N° du produit ABIN7318800

Détail du produit

Antigène: GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

Type de proteíne: Recombinant

Origine: Humain

Source: Human Cells

Purification/Conjugué: Cette GNS protéine est marqué à la His tag.

Fonction: Recombinant Human GNS Protein (His Tag)

Séquence: Val37-Leu552

Attributs du produit: Recombinant Human N-Acetylglucosamine-6-Sulfatase is produced by our Mammalian expression system and the target gene encoding Val37-Leu552 is expressed with a 6His tag at the C-terminus.

Pureté: > 95 % as determined by reducing SDS-PAGE.

niveau d'endotoxine: < 1.0 EU per μg as determined by the LAL method.

Information d'application

Restrictions: For Research Use only

Stockage

Format: Frozen, Liquid

Buffer: Supplied as a 0.2 μm filtered solution of 20 mM TrisHCl, 150 mM NaCl,10 % Glycerol, pH 8.0.

Stock: -20 °C

Stockage commentaire: Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.

Détail du antigène

Antigène: GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

Autre désignation: GNS (GNS Produits)

Synonymes: G6S Protein, 2610016K11Rik Protein, AU042285 Protein, C87209 Protein, N28088 Protein, NV14559 Protein, N-acetylglucosamine-6-sulfatase Protein, zgc:114066 Protein, gns Protein, wu:fi20h10 Protein, zgc:55370 Protein, glucosamine (N-acetyl)-6-sulfatase Protein, glucosamine (N-acetyl)-6-sulfatase S homeolog Protein, glucosamine (N-acetyl)-6-sulfatase a Protein, N-acetylglucosamine-6-sulfatase Protein, glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), b Protein, GNS Protein, Gns Protein, gns.S Protein, gns Protein, gnsa Protein, CpipJ_CPIJ000745 Protein, Sros_7372 Protein, VDBG_04409 Protein, Halhy_3165 Protein, gnsb Protein

Sujet:

Background: N-Acetylglucosamine-6-Sulfatase is a member of the Sulfatase family. N-Acetylglucosamine-6-Sulfatase is required for the lysosomal degradation of the Glycosaminoglycans (GAG) Heparan Sulfate and Keratan Sulfate. N-Acetylglucosamine-6-Sulfatase hydrolyzes the 6-Sulfate groups of the N-Acetyl-D-Glucosamine 6-Sulfate units of Heparan Sulfate and Keratan Sulfate. N-Acetylglucosamine-6-Sulfatase binds 1 Calcium ion per subunit. N-Acetylglucosamine-6-Sulfatase deficiency are the cause of Mucopolysaccharidosis Type 3D (MPS3D), an inborn error leading to lysosomal accumulation of heparan sulfate. MPS3D has profound mental deterioration, hyperactivity, and relatively mild somatic manifestations.

Synonym: N-Acetylglucosamine-6-Sulfatase, Glucosamine-6-Sulfatase, G6S, GNS

Poids moléculaire: 59.4 kDa

UniProt: P15586

Pathways: Glycosaminoglycan Metabolic Process