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Desmin antibody (AA 104-391)

This Mouse Monoclonal antibody specifically detects Desmin in WB, IHC and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN2719408

Quick Overview for Desmin antibody (AA 104-391) (ABIN2719408)

Target

See all Desmin (DES) Antibodies
Desmin (DES)

Reactivity

  • 195
  • 108
  • 88
  • 57
  • 40
  • 13
  • 13
  • 9
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  • 5
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  • 1
Human

Host

  • 133
  • 67
  • 2
Mouse

Clonality

  • 115
  • 87
  • 1
Monoclonal

Conjugate

  • 108
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  • 3
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  • 3
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  • 3
  • 3
  • 3
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  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Desmin antibody is un-conjugated

Application

  • 138
  • 111
  • 52
  • 44
  • 29
  • 27
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  • 22
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  • 13
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Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Clone

4G1
  • Binding Specificity

    • 16
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    • 1
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    • 1
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    • 1
    AA 104-391

    Characteristics

    Homo sapiens desmin (DES)

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Human fragment corresponding to amino acids 104-391 of human DES (NP_001918) produced in E.coli.

    Isotype

    IgG1
  • Application Notes

    WB 1:200~500, IHC 1:150, FLOW 1:100,

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    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
  • Target

    Desmin (DES)

    Alternative Name

    DES

    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.

    Molecular Weight

    53.4 kDa

    Gene ID

    1674

    NCBI Accession

    NM_001927

    HGNC

    1674
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