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AMPD3 antibody

AMPD3 Reactivity: Human IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6290008
  • Target See all AMPD3 Antibodies
    AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))
    Reactivity
    • 41
    • 23
    • 20
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 29
    • 12
    Rabbit
    Clonality
    • 28
    • 12
    Polyclonal
    Conjugate
    • 20
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AMPD3 antibody is un-conjugated
    Application
    • 26
    • 13
    • 12
    • 10
    • 10
    • 8
    • 7
    • 7
    • 6
    • 2
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human AMPD3
    Isotype
    IgG
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    Discover our top product AMPD3 Primary Antibody
  • Application Notes
    IF 1:50 - 1:200
    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Target
    AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))
    Alternative Name
    AMPD3 (AMPD3 Products)
    Synonyms
    ampd3 antibody, fi25h10 antibody, wu:fi25h10 antibody, zgc:55390 antibody, MGC108215 antibody, adenosine monophosphate deaminase 3 antibody, adenosine monophosphate deaminase 3b antibody, AMP deaminase 3 antibody, AMPD3 antibody, ampd3b antibody, PTRG_08116 antibody, ampd3 antibody, Ampd3 antibody
    Background
    This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described.
    Molecular Weight
    88.812 kDa
    Gene ID
    272
    UniProt
    Q01432
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