Anti-OCRL/INPP5b; clone N166A/26

Code: MABN609 D2-231

Analysis Note

ControlRat brain tissue lysate

Application

Research CategoryNeuroscience

Detect Inositol polyphosphate 5-phosphatase OCRL-1 u...


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Analysis Note

ControlRat brain tissue lysate

Application

Research CategoryNeuroscience

Detect Inositol polyphosphate 5-phosphatase OCRL-1 using this mouse monoclonal antibody, Anti-OCRL/INPP5b Antibody, clone N166A/26 validated for use in western blotting & IHC.

Research Sub CategoryDevelopmental Signaling

Western Blotting Analysis: 0.5 µg/mL from a representative lot detected OCRL/INPP5b in 10 µg of rat brain tissue lysate.
Western Blotting Analysis: A representative lot detected OCRL/INPP5b in COS cell lysates transiently transfected with GFP-tagged OCRL or RFP-tagged INPP5b, and demonstrated a loss of signal in COS cell lysates transiently transfected with untagged Kv2.1 plasmids (Prof. J. Trimmer, University of California, Davis.).
Immunohistochemistry Analysis: A 1:50-250 dilution from a representative lot detected OCRL/INPP5b in human cerebellum and human cardiac myocytes.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

General description

Inositol polyphosphate 5-phosphatase OCRL-1 (ORCL) is also called Lowe oculocerebrorenal syndrome protein. ORCL is a phosphotase that converts phosphatidylinositol 4,5-bisphosphate to phosphatidylinositol 4-phosphate, as well as inositol 1,4,5-trisphosphate to inositol 1,4-bisphosphate and inositol 1,3,4,5-tetrakisphosphate to inositol 1,3,4-trisphosphate. ORCL is involved in primary cilia assembly and may also have a role in lysosomal membrane trafficking. ORCL is expressed in brain, skeletal muscle, heart, kidney, lung, placenta, fibroblasts, retina and the retinal pigment epithelium. OCRL defects can cause Lowe oculocerebrorenal syndrome (OCRL) and Dent disease type 2 (DD2).

Immunogen

Recombinant protein corresponding to human OCRL/INPP5b.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Physical form

Purified mouse monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Protein G Purified

Format: Purified

Quality

Evaluated by Western Blotting in human brain tissue lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected OCRL/INPP5b in 10 µg of human brain tissue lysate.

Specificity

Cross-reacts with OCRL/INPP5b (Prof. J. Trimmer, Univerity of California, Davis).

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Target description

~104 kDa observed. Uncharacterized band(s) may appear in some lysates.

antibody formpurified immunoglobulin
antibody product typeprimary antibodies
biological sourcemouse
cloneN166A/26, monoclonal
Gene Informationhuman ... OCRL(4952)
isotypeIgG1κ
NCBI accession no.NP_000267
Quality Level100
shipped inwet ice
species reactivityhuman, rat
technique(s)western blot: suitable, immunohistochemistry: suitable
UniProt accession no.Q01968
This product has met the following criteria to qualify for the following awards:



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