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SGSH anticorps (AA 44-200)

SGSH Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1886470
  • Antigène Voir toutes SGSH Anticorps
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Épitope
    • 15
    • 13
    • 10
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 44-200
    Reactivité
    • 31
    • 19
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 43
    • 3
    • 1
    Lapin
    Clonalité
    • 46
    • 1
    Polyclonal
    Conjugué
    • 22
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SGSH est non-conjugé
    Application
    • 45
    • 17
    • 13
    • 13
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purified by Protein A.
    Immunogène
    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 44 and 200 of Human SGSH
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    Discover our top product SGSH Anticorps primaire
  • Indications d'application
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Agent conservateur
    Thimerosal (Merthiolate)
    Précaution d'utilisation
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Autre désignation
    SGSH (SGSH Produits)
    Synonymes
    anticorps HSS, anticorps MPS3A, anticorps SFMD, anticorps 4632406A19Rik, anticorps N-sulfoglucosamine sulfohydrolase, anticorps N-sulfoglucosamine sulfohydrolase (sulfamidase), anticorps SGSH, anticorps Sgsh
    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.[provided by RefSeq]
    Poids moléculaire
    57 kDa
    ID gène
    6448
    NCBI Accession
    NM_000199, NP_000190
    Pathways
    Glycosaminoglycan Metabolic Process
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