OCRL polyclonal, anti-human, mouse, rat
€295.00
In stock
SKU
K008057P
Catalog Number: K008057P
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: IHC
Request Manual
Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: IHC
Request Manual
Questions? Contact us!
Background:
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.
Synonyms: LOCR, NPHL2, OCRL1, INPP5F, OCRL-1
Cellular Location: Cytoplasm
Immunogen:
A synthetic peptide of human OCRL
Gene Symbol: OCRL
Gene ID: 4952
Swiss prot: Q01968
Calculated MW: 104kDa
Recommended dilution:
IHC 1:25-100
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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.
Synonyms: LOCR, NPHL2, OCRL1, INPP5F, OCRL-1
Cellular Location: Cytoplasm
Immunogen:
A synthetic peptide of human OCRL
Gene Symbol: OCRL
Gene ID: 4952
Swiss prot: Q01968
Calculated MW: 104kDa
Recommended dilution:
IHC 1:25-100
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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