Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

SGSH Protein (Myc-DYKDDDDK Tag)

SGSH Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2732936
  • Antigène Voir toutes SGSH Protéines
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 2
    Humain
    Source
    • 3
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette SGSH protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Sulphamidase / SGSH protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SGSH Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Autre désignation
    Sulphamidase,sgsh (SGSH Produits)
    Synonymes
    HSS Protein, MPS3A Protein, SFMD Protein, 4632406A19Rik Protein, N-sulfoglucosamine sulfohydrolase Protein, N-sulfoglucosamine sulfohydrolase (sulfamidase) Protein, SGSH Protein, Sgsh Protein
    Sujet
    This gene encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.
    Poids moléculaire
    54.6 kDa
    NCBI Accession
    NP_000190
    Pathways
    Glycosaminoglycan Metabolic Process
Vous êtes ici:
Support technique