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Desmin antibody

DES Reactivity: Human, Mouse, Rat IHC (p), IF Host: Mouse Monoclonal 7A6 unconjugated
Catalog No. ABIN7250302
  • Target See all Desmin (DES) Antibodies
    Desmin (DES)
    Reactivity
    • 153
    • 83
    • 81
    • 34
    • 18
    • 13
    • 12
    • 8
    • 8
    • 5
    • 4
    • 4
    • 2
    • 1
    Human, Mouse, Rat
    Host
    • 115
    • 38
    • 2
    Mouse
    Clonality
    • 109
    • 47
    Monoclonal
    Conjugate
    • 79
    • 8
    • 7
    • 6
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Desmin antibody is un-conjugated
    Application
    • 114
    • 67
    • 49
    • 45
    • 27
    • 21
    • 14
    • 13
    • 10
    • 8
    • 8
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
    Characteristics
    Monoclonal Antibody
    Purification
    Protein A purification
    Immunogen
    Recombinant Protein
    Clone
    7A6
    Isotype
    IgG
    Top Product
    Discover our top product DES 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, 0.5 % BSA and 50 % glycerol, pH 7.4
    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
    Desmin (DES)
    Alternative Name
    Desmin (DES Products)
    Background
    This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies.
    UniProt
    P17661
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