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erythrocyte Membrane Protein Band 4.9 (Dematin) (EPB49) (Middle Region) Peptide

EPB49 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN5512610

Quick Overview for erythrocyte Membrane Protein Band 4.9 (Dematin) (EPB49) (Middle Region) Peptide (ABIN5512610)

Target

Dematin (EPB49) (erythrocyte Membrane Protein Band 4.9 (Dematin) (EPB49))

Origin

Human

Source

  • 4
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Sequence

    SLPAYGRTTL SRLQSTEFSP SGSETGSPGL QNGEGQRGRM DRGNSLPCVL

    Characteristics

    This is a synthetic peptide designed for use in combination with anti- EPB49 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    Dematin (EPB49) (erythrocyte Membrane Protein Band 4.9 (Dematin) (EPB49))

    Background

    The protein encoded by this gene is an actin binding and bundling protein that plays a structural role in erythrocytes, by stabilizing and attaching the spectrin/actin cytoskeleton to the erythrocyte membrane in a phosphorylation-dependent manner. This protein contains a core domain in the N-terminus, and a headpiece domain in the C-terminus that binds F-actin. When purified from erythrocytes, this protein exists as a trimer composed of two 48 kDa polypeptides and a 52 kDa polypeptide. The different subunits arise from alternative splicing in the 3' coding region, where the headpiece domain is located. Disruption of this gene has been correlated with the autosomal dominant Marie Unna hereditary hypotrichosis disease, while loss of heterozygosity of this gene is thought to play a role in prostate cancer progression. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Alias Symbols: DMT, EPB49

    Protein Size: 365

    Gene ID

    2039

    NCBI Accession

    NM_001114135, NP_001107607
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