
WB analysis of HEK293T (A), SP2/0 (B), H9C2 (C) whole cell lysates using GTX56011 INPP5E antibody.
INPP5E antibody
GTX56011
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetINPP5E
Overview
- SupplierGeneTex
- Product NameINPP5E antibody
- Delivery Days Customer9
- Application Supplier NoteWB: 1:500 - 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsWestern Blot
- CertificationResearch Use Only
- ClonalityPolyclonal
- ConjugateUnconjugated
- Gene ID56623
- Target nameINPP5E
- Target descriptioninositol polyphosphate-5-phosphatase E
- Target synonyms72 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
- HostRabbit
- IsotypeIgG
- Protein IDQ9NRR6
- Protein Name72 kDa inositol polyphosphate 5-phosphatase
- Scientific DescriptionThe 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]
- ReactivityHuman, Mouse, Rat
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203