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GAA Protein (AA 595-770) (His tag)

GAA Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 97 % WB, SDS, Imm, PC
N° du produit ABIN1079658
  • Antigène Voir toutes GAA Protéines
    GAA (Glucosidase, Alpha, Acid (GAA))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 595-770
    Origine
    • 7
    • 4
    • 3
    Humain
    Source
    • 8
    • 4
    • 2
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette GAA protéine est marqué à la His tag.
    Application
    Western Blotting (WB), SDS-PAGE (SDS), Immunogen (Imm), Positive Control (PC)
    Séquence
    Pro595-Gly770
    Attributs du produit
    Residues: Ala761~Asn919 (Accession # P10253), with N-terminal His-Tag.
    Pureté
    > 97 %
    Top Product
    Discover our top product GAA Protéine
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Commentaires

    Isoelectric Point:6.2

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    PBS, pH 7.4, containing 0.01 % SKL, 1 mM DTT, 5 % Trehalose and Proclin300.
    Agent conservateur
    ProClin
    Stock
    4 °C,-80 °C
    Stockage commentaire
    Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months.
    Date de péremption
    12 months
  • Antigène
    GAA (Glucosidase, Alpha, Acid (GAA))
    Autre désignation
    Glucosidase Alpha, Acid (GAA Produits)
    Synonymes
    LYAG Protein, E430018M07Rik Protein, glucosidase alpha, acid Protein, glucosidase, alpha, acid Protein, transmembrane and coiled-coil domain family 1 Protein, glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) Protein, GAA Protein, Gaa Protein, TMCC1 Protein, gaa Protein
    Sujet
    LYAG, Acid Alpha-Glucosidase, Lysosomal Alpha-Glucosidase, Pompe Disease Glycogen Storage Disease Type II, Acid Maltase, Aglucosidase Alfa
    Poids moléculaire
    18.53 kDa
    UniProt
    P10253
    Pathways
    Cellular Glucan Metabolic Process
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