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AGXT anticorps

AGXT Reactivité: Humain, Souris, Rat WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2426537
  • Antigène Voir toutes AGXT Anticorps
    AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 33
    • 6
    • 2
    Lapin
    Clonalité
    • 35
    • 6
    Polyclonal
    Conjugué
    • 22
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AGXT est non-conjugé
    Application
    • 21
    • 18
    • 13
    • 11
    • 5
    • 4
    • 4
    • 4
    • 2
    Western Blotting (WB), ELISA
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human AGXT
    Isotype
    IgG
    Top Product
    Discover our top product AGXT Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.6 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
    Autre désignation
    AGXT (AGXT Produits)
    Synonymes
    anticorps AGT, anticorps AGT1, anticorps AGXT1, anticorps PH1, anticorps SPAT, anticorps SPT, anticorps TLH6, anticorps Spat, anticorps Agt1, anticorps Agxt1, anticorps agt, anticorps agt1, anticorps agxt, anticorps agxt1, anticorps spt, anticorps agxtl, anticorps zgc:91879, anticorps wu:fb57d01, anticorps zgc:65930, anticorps alanine-glyoxylate aminotransferase, anticorps serine--pyruvate aminotransferase, mitochondrial, anticorps alanine-glyoxylate aminotransferase L homeolog, anticorps alanine-glyoxylate aminotransferase a, anticorps alanine-glyoxylate aminotransferase b, anticorps AGXT, anticorps Agxt, anticorps LOC607355, anticorps agxt.L, anticorps agxta, anticorps agxtb
    Sujet
    AGT,AGT1,Agxt,AGXT1,Alanine glyoxylate aminotransferase,Alanine glyoxylate aminotransferase3,Alanine--glyoxylate aminotransferase,EC 2.6.1.44,EC 2.6.1.51,Hepatic peroxisomal alanine glyoxylate aminotransferase,Hepatic peroxisomal alanine:glyoxylate aminotransferase,L alanine glyoxylate aminotransferase 1,MS773,PH1,Serine pyruvate aminotransferase,Serine--pyruvate aminotransferase,Serine--pyruvate aminotransferase,mitochondrial,Serine:pyruvate aminotransferase,SPAT,SPT,SPYA,TLH6,Serine-pyruvate aminotransferase is an enzyme that in humans is encoded by the AGXT gene. This gene is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I primary hyperoxaluria. Defects in AGXT are the cause of hyperoxaluria primary type 1 (HP1), also known as primary hyperoxaluria type I (PH1) and oxalosis I. HP1 is a rare autosomal recessive inborn error of glyoxylate metabolism characterized by increased excretion of oxalate and glycolate, and the progressive accumulation of insoluble calcium oxalate in the kidney and urinary tract.
    Poids moléculaire
    Calculated MW: 43 kDa
    NCBI Accession
    NP_000021
    Pathways
    Monocarboxylic Acid Catabolic Process, Dicarboxylic Acid Transport
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