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AMPD1 antibody

AMPD1 Reactivity: Human ELISA, WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7238522
  • Target See all AMPD1 Antibodies
    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
    Reactivity
    • 29
    • 22
    • 21
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Human
    Host
    • 35
    • 1
    Rabbit
    Clonality
    • 36
    Polyclonal
    Conjugate
    • 12
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AMPD1 antibody is un-conjugated
    Application
    • 13
    • 13
    • 11
    • 8
    • 6
    • 3
    • 1
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human AMPD1
    Isotype
    IgG
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    Discover our top product AMPD1 Primary Antibody
  • Application Notes
    WB 1:1000-1:5000, IHC 1:100-1:300
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 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
    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
    Alternative Name
    AMPD1 (AMPD1 Products)
    Background
    Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.
    Molecular Weight
    90 kDa
    NCBI Accession
    NP_000027
    UniProt
    P23109
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