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SGCE antibody (AA 38-407)

The Rabbit Polyclonal anti-SGCE antibody is suitable to detect SGCE in samples from Human, Mouse and Rat. It has been validated for WB, ELISA, IHC (p) and FACS.
Catalog No. ABIN7874505
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SGCE antibody (AA 38-407) (ABIN7874505)

Target

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

Reactivity

  • 26
  • 23
  • 21
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 41
  • 2
Rabbit

Clonality

  • 43
Polyclonal

Conjugate

  • 20
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  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SGCE antibody is un-conjugated

Application

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  • 13
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  • 9
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  • 5
  • 4
  • 2
  • 1
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  • 1
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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 4
    • 4
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    • 2
    • 2
    • 2
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    AA 38-407

    Purpose

    SGCE Antibody / Epsilon-sarcoglycan

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids Y38-D407) was used as the immunogen for the SGCE antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SGCE antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the SGCE antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    SGCE (Sarcoglycan, epsilon (SGCE))

    Alternative Name

    SGCE

    Background

    Epsilon-sarcoglycan is a protein that in humans is encoded by the SGCE gene. This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A pseudogene associated with this gene is located on chromosome 2.

    UniProt

    O43556
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