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TIMM17A antibody

TIMM17A Reactivity: Human, Mouse IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7257184
  • Target See all TIMM17A Antibodies
    TIMM17A (Translocase of Inner Mitochondrial Membrane 17 Homolog A (TIMM17A))
    Reactivity
    • 46
    • 24
    • 15
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse
    Host
    • 46
    Rabbit
    Clonality
    • 46
    Polyclonal
    Conjugate
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TIMM17A antibody is un-conjugated
    Application
    • 30
    • 13
    • 13
    • 6
    • 6
    • 5
    • 5
    • 4
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human TIMM17A (NP_006326.1).
    Isotype
    IgG
    Top Product
    Discover our top product TIMM17A Primary Antibody
  • Application Notes
    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
    TIMM17A (Translocase of Inner Mitochondrial Membrane 17 Homolog A (TIMM17A))
    Alternative Name
    TIMM17A (TIMM17A Products)
    Synonyms
    TIM17 antibody, TIM17A antibody, Tim17 antibody, Timm17 antibody, 17kDa antibody, mTim17a antibody, translocase of inner mitochondrial membrane 17A antibody, translocase of inner mitochondrial membrane 17a antibody, TIMM17A antibody, Timm17a antibody
    Background
    TIMM17A (Translocase Of Inner Mitochondrial Membrane 17A) is a Protein Coding gene. Diseases associated with TIMM17A include Barth Syndrome and Mohr-Tranebjaerg Syndrome. Among its related pathways are Metabolism of proteins and Mitochondrial protein import. Gene Ontology (GO) annotations related to this gene include P-P-bond-hydrolysis-driven protein transmembrane transporter activity. An important paralog of this gene is TIMM17B.
    Gene ID
    10440
    UniProt
    Q99595
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