OCRL rabbit pAb
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],
Product Specifications
Background
Product Name Alternative
OCRL; INPP5F; OCRL1; Inositol polyphosphate 5-phosphatase OCRL-1; Lowe oculocerebrorenal syndrome protein
UniProt
Q01968
Swiss Prot
Q01968
Reactivity
Human; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human OCRL. AA range:150-199
Target
OCRL
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
Buffer
-20°C/1 year
Molecular Weight
104kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
104kD
Fragment
IgG
Subcellular Location
Other Product Names
OCRL; INPP5F; OCRL1; Inositol polyphosphate 5-phosphatase OCRL-1; Lowe oculocerebrorenal syndrome protein
Gene ID (Human)
4952
Available Sizes
Frequently Asked Questions
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