Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

SGCE antibody

The Rabbit Polyclonal anti-SGCE antibody has been validated for WB, ELISA, IHC and IF. It is suitable to detect SGCE in samples from Human and Mouse.
Catalog No. ABIN7118789

Quick Overview for SGCE antibody (ABIN7118789)

Target

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

Reactivity

  • 25
  • 22
  • 21
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 38
  • 2
Rabbit

Clonality

  • 40
Polyclonal

Conjugate

  • 17
  • 2
  • 2
  • 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

  • 30
  • 13
  • 13
  • 8
  • 5
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    sarcoglycan, epsilon

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    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

    Storage Comment

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    SGCE (Sarcoglycan, epsilon (SGCE))

    Alternative Name

    SGCE

    Background

    Synonyms:ESG Background: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.

    Molecular Weight

    55 kDa

    Gene ID

    8910

    UniProt

    O43556
You are here:
Chat with us!