GNS Protein (AA 37-552) (His tag)

N° du produit ABIN1096744

Détail du produit

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

Type de proteíne: Recombinant

Attributs du protein: AA 37-552

Origine: Humain

Source: Human Cells

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

Fonction: Recombinant Human N-Acetylglucosamine-6-Sulfatase/GNS (C-6His)

Séquence: VFGVAAGTRR PNVVLLLTDD QDEVLGGMTP LKKTKALIGE MGMTFSSAYV PSALCCPSRA SILTGKYPHN HHVVNNTLEG NCSSKSWQKI QEPNTFPAIL RSMCGYQTFF AGKYLNEYGA PDAGGLEHVP LGWSYWYALE KNSKYYNYTL SINGKARKHG ENYSVDYLTD VLANVSLDFL DYKSNFEPFF MMIATPAPHS PWTAAPQYQK AFQNVFAPRN KNFNIHGTNK HWLIRQAKTP MTNSSIQFLD NAFRKRWQTL LSVDDLVEKL VKRLEFTGEL NNTYIFYTSD NGYHTGQFSL PIDKRQLYEF DIKVPLLVRG PGIKPNQTSK MLVANIDLGP TILDIAGYDL NKTQMDGMSL LPILRGASNL TWRSDVLVEY QGEGRNVTDP TCPSLSPGVS QCFPDCVCED AYNNTYACVR TMSALWNLQY CEFDDQEVFV EVYNLTADPD QITNIAKTID PELLGKMNYR LMMLQSCSGP TCRTPGVFDP GYRFDPRLMF SNRGSVRTRR FSKHLLVDHH HHHH

Attributs du produit:

Recombinant Human N-Acetylglucosamine-6-Sulfatase/GNS (C-6His)

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

Stérilité: 0.2 μm filtered

niveau d'endotoxine: Less than 0.1 ng/μg (1 IEU/μg) as determined by LAL test

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Reconstitution: It is not recommended to reconstitute to a concentration less than 100 μg/mL.
Dissolve the lyophilized protein in ddH2O.
Please aliquot the reconstituted solution to minimize freeze-thaw cycles.

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

Conseil sur la manipulation: Always centrifuge tubes before opening. Do not mix by vortex or pipetting.

Stock: -80 °C

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

Date de péremption: 6 months

Détail du antigène

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

Autre désignation: N-Acetylglucosamine-6-Sulfatase/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: Recombinant Human N-Acetylglucosamine-6-Sulfatase/GNS is produced by our mammalian expression system in human cells. The target protein is expressed with sequence (Val37-Leu552) of Human GNS fused with a polyhistidine tag at the C-terminus.
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.

Poids moléculaire: 59.35 kDa

UniProt: P15586

Pathways: Glycosaminoglycan Metabolic Process