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AGXT antibody

AGXT Reactivity: Human, Mouse, Rat WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7384024
  • Target See all AGXT Antibodies
    AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
    Reactivity
    Human, Mouse, Rat
    Host
    • 33
    • 5
    • 2
    Rabbit
    Clonality
    • 35
    • 5
    Polyclonal
    Conjugate
    • 21
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AGXT antibody is un-conjugated
    Application
    • 20
    • 17
    • 13
    • 10
    • 4
    • 4
    • 4
    • 3
    • 2
    Western Blotting (WB), ELISA
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human AGXT
    Isotype
    IgG
    Top Product
    Discover our top product AGXT Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Concentration
    0.6 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
    Alternative Name
    AGXT (AGXT Products)
    Synonyms
    AGT antibody, AGT1 antibody, AGXT1 antibody, PH1 antibody, SPAT antibody, SPT antibody, TLH6 antibody, Spat antibody, Agt1 antibody, Agxt1 antibody, agt antibody, agt1 antibody, agxt antibody, agxt1 antibody, spt antibody, agxtl antibody, zgc:91879 antibody, wu:fb57d01 antibody, zgc:65930 antibody, alanine-glyoxylate aminotransferase antibody, serine--pyruvate aminotransferase, mitochondrial antibody, alanine-glyoxylate aminotransferase L homeolog antibody, alanine-glyoxylate aminotransferase a antibody, alanine-glyoxylate aminotransferase b antibody, AGXT antibody, Agxt antibody, LOC607355 antibody, agxt.L antibody, agxta antibody, agxtb antibody
    Background
    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.
    Molecular Weight
    43 kDa
    NCBI Accession
    NP_000021
    UniProt
    P21549
    Pathways
    Monocarboxylic Acid Catabolic Process, Dicarboxylic Acid Transport
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