OCRL antibody (AA 1-901) (Cy3)
Quick Overview for OCRL antibody (AA 1-901) (Cy3) (ABIN8017917)
Target
See all OCRL AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 1-901
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Purpose
- Anti-OCRL Antibody Cy3 Conjugated
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins.
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human OCRL recombinant protein (Position: M1-D901).
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Isotype
- IgG
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Application Notes
- Flow Cytometry, 1-3 μg/1x106 cells
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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Expiry Date
- 12 months
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- OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
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Alternative Name
- OCRL
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Background
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Background: Inositol polyphosphate 5-phosphatase OCRL-1, also known as Lowe oculocerebrorenal syndrome protein, is an enzyme encoded by the OCRL gene located on the X chromosome in humans. 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.
Gene Full Name: OCRL inositol polyphosphate-5-phosphatase
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Gene ID
- 4952
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UniProt
- Q01968
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Pathways
- Inositol Metabolic Process
Target
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