INPP5E antibody

Cannot supply to this region.

SKU:: GTX56011
Additional Names:: inositol polyphosphate-5-phosphatase E , CORS1 , CPD4 , JBTS1 , MORMS , PPI5PIV , pharbin
Application:: WB
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Affinity Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Rabbit
Reactivities:: Human, Mouse, Rat
Buffer:: 0.42% Potassium Phosphate, 0.87% NaCl, 30% Glycerol, 0.01% Sodium azide.
Immunogen:: KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of INPP5E. The exact sequence is proprietary.
Uniprot:: Q9NRR6
Synonyms:: 72 kDa inositol polyphosphate 5-phosphatase;CORS1;CPD4;JBTS1;MORMS;pharbin;Phosphatidylinositol 4,5-bisphosphate 5-phosphatase;phosphatidylinositol polyphosphate 5-phosphatase type IV;phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase;phosphatidylinositol-4,5-bisphosphate 5-phosphatase;PPI5PIV
Extra Details:: 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]

Shipping Conditions:: Blue Ice