ARG45313

anti-OCRL antibody

anti-OCRL antibody for ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Polyclonal antibody recognizes OCRL
Tested Reactivity Hu
Tested Application ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Target Name OCRL
Antigen Species Human
Immunogen Recombinant protein containing to human OCRL.
Conjugation Un-conjugated
Alternate Names OCRL; OCRL Inositol Polyphosphate-5-Phosphatase; OCRL1; Dent-2; Phosphatidylinositol 3,4,5-Triphosphate 5-Phosphatase; Inositol Polyphosphate 5-Phosphatase OCRL-1; Inositol Polyphosphate 5-Phosphatase OCRL; Lowe Oculocerebrorenal Syndrome Protein; Oculocerebrorenal Syndrome Of Lowe; OCRL-1; Phosphatidylinositol Polyphosphate 5-Phosphatase; Dent Disease 2; EC 3.1.3.36; EC 3.1.3.56; EC 3.1.3.86; INPP5F; DENT2; NPHL2; LOCR

Application Instructions

Application Suggestion
Tested Application Dilution
ICC/IF5 μg/ml
IHC-P2-5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 104 kDa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 4952 Human OCRL

Swiss-port # Q01968 Human Inositol polyphosphate 5-phosphatase OCRL-1

Gene Symbol OCRL
Gene Full Name OCRL Inositol Polyphosphate-5-Phosphatase
Background This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016] GeneCards Summary for OCRL Gene
Function Catalyzes the hydrolysis of the 5-position phosphate of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) and phosphatidylinositol-3,4,5-bisphosphate (PtdIns(3,4,5)P3), with the greatest catalytic activity towards PtdIns(4,5)P2 . [UniProt]
Cellular Localization Cell projection; Cilium; Coated pit; Cytoplasmic vesicle; Endosome; Golgi apparatus; Lysosome; Membrane. [UniProt]
Calculated MW 104 kDa