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AGXT2L2 anticorps

AGXT2L2 Reactivité: Humain, Souris WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7235763
  • Antigène Voir toutes AGXT2L2 Anticorps
    AGXT2L2 (Alanine-Glyoxylate Aminotransferase 2-Like 2 (AGXT2L2))
    Reactivité
    • 35
    • 26
    • 25
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Humain, Souris
    Hôte
    • 33
    • 2
    Lapin
    Clonalité
    • 35
    Polyclonal
    Conjugué
    • 14
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AGXT2L2 est non-conjugé
    Application
    • 29
    • 13
    • 5
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human AGXT2L2
    Isotype
    IgG
    Top Product
    Discover our top product AGXT2L2 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.2 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    AGXT2L2 (Alanine-Glyoxylate Aminotransferase 2-Like 2 (AGXT2L2))
    Autre désignation
    PHYKPL (AGXT2L2 Produits)
    Synonymes
    anticorps AGXT2L2, anticorps PHLU, anticorps Agxt2l2, anticorps 2900006B13Rik, anticorps 5-phosphohydroxy-L-lysine phospho-lyase, anticorps 5-phosphohydroxy-L-lysine phospholyase, anticorps PHYKPL, anticorps phykpl, anticorps Phykpl
    Sujet
    This is a nuclear gene encoding a mitochondrial enzyme that catalyzes the conversion of 5-phosphonooxy-L-lysine to ammonia, inorganic phosphate, and 2-aminoadipate semialdehyde. Mutations in this gene may cause phosphohydroxylysinuria. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    50 kDa
    UniProt
    Q8IUZ5
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