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ETHE1 antibody

ETHE1 Reactivity: Human, Mouse, Rat WB, IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7255167
  • Target See all ETHE1 Antibodies
    ETHE1 (Ethylmalonic Encephalopathy 1 (ETHE1))
    Reactivity
    • 41
    • 17
    • 2
    • 2
    • 2
    • 2
    • 2
    Human, Mouse, Rat
    Host
    • 39
    • 2
    Rabbit
    Clonality
    • 41
    Polyclonal
    Conjugate
    • 16
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ETHE1 antibody is un-conjugated
    Application
    • 15
    • 13
    • 13
    • 10
    • 8
    • 6
    • 3
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ETHE1 (NP_055112.2).
    Isotype
    IgG
    Top Product
    Discover our top product ETHE1 Primary Antibody
  • Application Notes
    WB 1:200-1:1000 IHC 1:50-1:200 IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    ETHE1 (Ethylmalonic Encephalopathy 1 (ETHE1))
    Alternative Name
    ETHE1 (ETHE1 Products)
    Synonyms
    zgc:85680 antibody, HSCO antibody, YF13H12 antibody, 0610025L15Rik antibody, Hsco antibody, ETHE1, persulfide dioxygenase antibody, ethylmalonic encephalopathy 1 antibody, Ethe1 antibody, ethe1 antibody, ETHE1 antibody
    Background
    This gene encodes a member of the metallo beta-lactamase family of iron-containing proteins involved in the mitochondrial sulfide oxidation pathway. The encoded protein catalyzes the oxidation of a persulfide substrate to sulfite. Certain mutations in this gene cause ethylmalonic encephalopathy, an infantile metabolic disorder affecting the brain, gastrointestinal tract and peripheral vessels. Alternative splicing results in multiple transcript variants encoding different isoforms.
    Molecular Weight

    Observed_MW: 28 kDa

    Calculated_MW: 27 kDa

    Gene ID
    23474
    UniProt
    O95571
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