Product Name
Inositol Polyphosphate 5-Phosphatase OCRL-1 (OCRL), ELISA Kit
Full Product Name
Pigeon Inositol Polyphosphate 5-Phosphatase OCRL-1 (OCRL) ELISA Kit
Product Gene Name
OCRL elisa kit
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
3D Structure
ModBase 3D Structure for Q01968
Species Reactivity
Pigeon
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of OCRL elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for OCRL purchase
MBS9396950 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Inositol Polyphosphate 5-Phosphatase OCRL-1 (OCRL) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing OCRL. The ELISA analytical biochemical technique of the MBS9396950 kit is based on OCRL antibody-OCRL antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect OCRL antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, OCRL. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for OCRL. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001305713.1
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NCBI GenBank Nucleotide #
NM_001318784.1
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UniProt Primary Accession #
Q01968
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UniProt Secondary Accession #
O60800; Q15684; Q15774; Q4VY09; Q4VY10; Q5JQF1; Q5JQF2; Q9UJG5; A6NKI1; A8KAP2; B7ZLX2[Other Products]
UniProt Related Accession #
Q01968[Other Products]
Molecular Weight
103,227 Da
NCBI Official Full Name
inositol polyphosphate 5-phosphatase OCRL-1 isoform c
NCBI Official Synonym Full Names
OCRL, inositol polyphosphate-5-phosphatase
NCBI Official Symbol
OCRL [Similar Products]
NCBI Official Synonym Symbols
LOCR; NPHL2; OCRL1; INPP5F; OCRL-1
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NCBI Protein Information
inositol polyphosphate 5-phosphatase OCRL-1
UniProt Protein Name
Inositol polyphosphate 5-phosphatase OCRL-1
UniProt Synonym Protein Names
Lowe oculocerebrorenal syndrome protein
Protein Family
Inositol polyphosphate 5-phosphatase
UniProt Gene Name
OCRL [Similar Products]
UniProt Synonym Gene Names
INPP5F; OCRL1 [Similar Products]
NCBI Summary for OCRL
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]
UniProt Comments for OCRL
OCRL: Converts phosphatidylinositol 4,5-bisphosphate to phosphatidylinositol 4-phosphate. Also converts inositol 1,4,5- trisphosphate to inositol 1,4-bisphosphate and inositol 1,3,4,5- tetrakisphosphate to inositol 1,3,4-trisphosphate. May function in lysosomal membrane trafficking by regulating the specific pool of phosphatidylinositol 4,5-bisphosphate that is associated with lysosomes. Belongs to the inositol-1,4,5-trisphosphate 5- phosphatase type II family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Carbohydrate Metabolism - inositol phosphate; EC 3.1.3.36; Motility/polarity/chemotaxis; Phosphatase (non-protein)
Chromosomal Location of Human Ortholog: Xq26.1
Cellular Component: clathrin-coated pit; clathrin-coated vesicle; cytoplasm; cytosol; early endosome; early endosome membrane; Golgi stack; Golgi-associated vesicle; nucleus; phagocytic vesicle membrane; photoreceptor outer segment; plasma membrane; trans-Golgi network
Molecular Function: GTPase activator activity; phosphatidylinositol-3,5-bisphosphate 5-phosphatase activity; phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity; protein binding; Rac GTPase binding
Biological Process: in utero embryonic development; inositol phosphate metabolic process; lipid metabolic process; phosphatidylinositol biosynthetic process; phosphatidylinositol dephosphorylation; positive regulation of GTPase activity; regulation of GTPase activity; regulation of small GTPase mediated signal transduction; signal transduction
Disease: Dent Disease 2; Lowe Oculocerebrorenal Syndrome
Research Articles on OCRL
1. OCRL1 gene mutation is responsible in the development od Lowe syndrome in Chinese families.
Precautions
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