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Emerin antibody (AA 1-222)

EMD Reactivity: Human ELISA, IHC, FACS, ICC Host: Mouse Monoclonal 8F5A8 unconjugated
Catalog No. ABIN5542309
  • Target See all Emerin (EMD) Antibodies
    Emerin (EMD)
    Binding Specificity
    • 15
    • 8
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-222
    Reactivity
    • 59
    • 16
    • 13
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 48
    • 11
    • 2
    Mouse
    Clonality
    • 48
    • 13
    Monoclonal
    Conjugate
    • 35
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Emerin antibody is un-conjugated
    Application
    • 48
    • 16
    • 13
    • 13
    • 13
    • 9
    • 9
    • 7
    • 6
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC)
    Purpose
    EMD Antibody
    Purification
    Purified antibody
    Immunogen
    Purified recombinant fragment of human EMD (AA: 1-222) expressed in E. Coli.
    Clone
    8F5A8
    Isotype
    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified antibody in PBS with 0.05 % 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
    4 °C,-20 °C
    Storage Comment
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target
    Emerin (EMD)
    Alternative Name
    EMD (EMD Products)
    Background

    Description: Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.

    Aliases: STA, EDMD, LEMD5

    Molecular Weight
    29kDa
    Gene ID
    2010
    HGNC
    2010
    UniProt
    P50402
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