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HAL antibody (AA 1-200)

HAL Reactivity: Human WB, IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6141593
  • Target See all HAL Antibodies
    HAL (Histidine Ammonia-Lyase (HAL))
    Binding Specificity
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    AA 1-200
    Reactivity
    • 19
    • 9
    • 8
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    Host
    • 16
    • 3
    Rabbit
    Clonality
    • 18
    • 1
    Polyclonal
    Conjugate
    • 15
    • 2
    • 1
    • 1
    This HAL antibody is un-conjugated
    Application
    • 14
    • 8
    • 6
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    Sequence
    MPRYTVHVRG EWLAVPCQDA QLTVGWLGRE AVRRYIKNKP DNGGFTSVDD AHFLVRRCKG LGLLDNEDRL EVALENNEFV EVVIEGDAMS PDFIPSQPEG VYLYSKYREP EKYIELDGDR LTTEDLVNLG KGRYKIKLTP TAEKRVQKSR EVIDSIIKEK TVVYGITTGF GKFARTVIPI NKLQELQVNL VRSHSSGVGK
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-200 of human HAL (NP_002099.1).
    Isotype
    IgG
    Top Product
    Discover our top product HAL Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:100
    Comment

    HIGH QUALITY

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    HAL (Histidine Ammonia-Lyase (HAL))
    Alternative Name
    HAL (HAL Products)
    Background
    Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids. Several transcript variants encoding different isoforms have been found for this gene.,HAL,HIS,HSTD,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,HAL
    Molecular Weight
    49 kDa/64 kDa/72 kDa
    Gene ID
    3034
    UniProt
    P42357
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