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

EPB49 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN5512610
发货至: 中国
  • 抗原 See all Dematin (EPB49) products
    Dematin (EPB49) (erythrocyte Membrane Protein Band 4.9 (Dematin) (EPB49))
    蛋白结构域
    Middle Region
    宿主
    资源
    • 4
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    SLPAYGRTTL SRLQSTEFSP SGSETGSPGL QNGEGQRGRM DRGNSLPCVL
    产品特性
    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.
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    Dematin (EPB49) (erythrocyte Membrane Protein Band 4.9 (Dematin) (EPB49))
    别名
    MGC80597 Peptide, MGC108072 Peptide, EPB49 Peptide, DMT Peptide, AI325486 Peptide, Epb4.9 Peptide, Epb49 Peptide, dematin Peptide, dematin actin binding protein L homeolog Peptide, dematin actin binding protein Peptide, dmtn.L Peptide, DMTN Peptide, dmtn Peptide, Dmtn Peptide
    背景
    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
    基因ID
    2039
    NCBI登录号
    NM_001114135, NP_001107607
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