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WB analysis of HEK293T (A), SP2/0 (B), H9C2 (C) whole cell lysates using GTX56011 INPP5E antibody.
WB analysis of HEK293T (A), SP2/0 (B), H9C2 (C) whole cell lysates using GTX56011 INPP5E antibody.
WB analysis of HEK293T (A), SP2/0 (B), H9C2 (C) whole cell lysates using GTX56011 INPP5E antibody.

INPP5E antibody

GTX56011
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetINPP5E
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Overview

  • Supplier
    GeneTex
  • Product Name
    INPP5E antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID56623
  • Target name
    INPP5E
  • Target description
    inositol polyphosphate-5-phosphatase E
  • Target synonyms
    72 kDa inositol polyphosphate 5-phosphatase; CORS1; CPD4; JBTS1; MORMS; pharbin; phosphatidylinositol polyphosphate 5-phosphatase type IV; phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase; phosphatidylinositol-4,5-bisphosphate 5-phosphatase; PPI5PIV
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NRR6
  • Protein Name
    72 kDa inositol polyphosphate 5-phosphatase
  • Scientific Description
    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. [provided by RefSeq, Jan 2016]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203