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Emerin antibody

The Rabbit Polyclonal anti-Emerin antibody has been validated for WB, IF, ICC and IHC (p). It is suitable to detect Emerin in samples from Human.
Catalog No. ABIN7464517

Quick Overview for Emerin antibody (ABIN7464517)

Target

See all Emerin (EMD) Antibodies
Emerin (EMD)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Emerin antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Grade

KO Validated
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Emerin. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:1000-1:10000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: HeLa nucleus , 293T

    Validation: KO/KD

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    Emerin (EMD)

    Alternative Name

    emerin

    Background

    Emerin , EDMD , LEMD5 , STA,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. [provided by RefSeq]

    Molecular Weight

    29 kDa

    Gene ID

    2010

    UniProt

    P50402
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