OCRL Protein (Transcript Variant A) (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes OCRL Protéines
- OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
- Type de proteíne
- Recombinant
- Attributs du protein
- Transcript Variant A
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette OCRL protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human OCRL (transcript variant a) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product OCRL Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Antigène
- OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
- Autre désignation
- Ocrl (OCRL Produits)
- Synonymes
- OCRL Protein, wu:fi09g03 Protein, zgc:152864 Protein, locr Protein, nphl2 Protein, ocrl1 Protein, inpp5f Protein, INPP5F Protein, LOCR Protein, NPHL2 Protein, OCRL-1 Protein, OCRL1 Protein, 9530014D17Rik Protein, BB143339 Protein, OCRL, inositol polyphosphate-5-phosphatase Protein, phosphatidylinositol polyphosphate 5-phosphatase Protein, oculocerebrorenal syndrome of Lowe Protein, Ocrl Protein, NAEGRDRAFT_58601 Protein, OCRL Protein, ocrl Protein
- Sujet
- 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.
- Poids moléculaire
- 104 kDa
- NCBI Accession
- NP_000267
- Pathways
- Inositol Metabolic Process
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