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TUFM antibody

Tufm Reactivity: Human, Mouse, Rat IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6570431
  • Target See all TUFM (Tufm) Antibodies
    TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
    Reactivity
    • 60
    • 14
    • 8
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 55
    • 5
    Rabbit
    Clonality
    • 57
    • 3
    Polyclonal
    Conjugate
    • 31
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This TUFM antibody is un-conjugated
    Application
    • 42
    • 22
    • 8
    • 7
    • 5
    • 4
    • 3
    • 2
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human TUFM (NP_003312.3).
    Isotype
    IgG
    Top Product
    Discover our top product Tufm Primary Antibody
  • Application Notes
    IHC 1:50-1:200 IF 1:10-1:100
    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
    TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
    Alternative Name
    TUFM (Tufm Products)
    Synonyms
    TUFM antibody, D250 antibody, fi06f04 antibody, wu:fi06f04 antibody, zgc:110766 antibody, COXPD4 antibody, EF-TuMT antibody, EFTU antibody, P43 antibody, 2300002G02Rik antibody, C76308 antibody, C76389 antibody, Tu translation elongation factor, mitochondrial antibody, TUFM antibody, tufm antibody, Tufm antibody
    Background
    This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.
    Molecular Weight

    Observed_MW: 48kDa

    Calculated_MW: 49kDa

    Gene ID
    7284
    UniProt
    P49411
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