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SGCE antibody

This anti-SGCE antibody is a Rabbit Polyclonal antibody detecting SGCE in WB and IHC (p). Suitable for Human.
Catalog No. ABIN7465874

Quick Overview for SGCE antibody (ABIN7465874)

Target

See all SGCE Antibodies
SGCE (Sarcoglycan, epsilon (SGCE))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This SGCE antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human, Mouse

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: HeLa

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 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

    SGCE (Sarcoglycan, epsilon (SGCE))

    Alternative Name

    sarcoglycan epsilon

    Background

    Sarcoglycan epsilon , DYT11 , ESG , epsilon-SG,This gene encodes a member of the sarcoglycan family. Sarcoglycans are transmembrane components in the dystrophin-glycoprotein complex which help stabilize the muscle fiber membranes and link the muscle cytoskeleton to the extracellular matrix. Mutations in this gene have been associated with myoclonus-dystonia syndrome. Alternative splicing results in multiple transcript variants.

    Molecular Weight

    50 kDa

    Gene ID

    8910

    UniProt

    O43556
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