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Inositol Polyphosphate-5-Phosphatase, 72 KDa (INPP5E) (Middle Region) Peptide

INPP5E 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN5513259
发货至: 中国
  • 抗原 See all INPP5E products
    INPP5E (Inositol Polyphosphate-5-Phosphatase, 72 KDa (INPP5E))
    蛋白结构域
    Middle Region
    宿主
    资源
    • 1
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    SLQEIPKSRG VLSSERGSPS SGGNPLSGVA SSSPNLPHRD AAVAGSSPRL
    产品特性
    This is a synthetic peptide designed for use in combination with anti- INPP5E 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
    INPP5E (Inositol Polyphosphate-5-Phosphatase, 72 KDa (INPP5E))
    别名
    1200002L24Rik Peptide, 72kDa Peptide, mKIAA0123 Peptide, CORS1 Peptide, CPD4 Peptide, JBTS1 Peptide, MORMS Peptide, PPI5PIV Peptide, PMPCA Peptide, inositol polyphosphate-5-phosphatase E Peptide, Inpp5e Peptide, INPP5E Peptide
    背景
    The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. InsP3 5-phosphatases hydrolyze Ins(1,4,5)P3, which mobilizes intracellular calcium and acts as a second messenger mediating cell responses to various stimulation. Studies of the mouse counterpart suggest that this protein may hydrolyze phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,5-bisphosphate on the cytoplasmic Golgi membrane and thereby regulate Golgi-vesicular trafficking. Mutations in this gene cause Joubert syndrome, a clinically and genetically heterogenous group of disorders characterized by midbrain-hindbrain malformation and various associated ciliopathies that include retinal dystrophy, nephronophthisis, liver fibrosis and polydactyly. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Alias Symbols: CPD4, CORS1, JBTS1, MORMS, PPI5PIV

    Protein Size: 610
    基因ID
    56623
    NCBI登录号
    NM_019892, NP_063945
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