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Mutations in this gene are associated with erythrocytosis familial type 3 (ECYT3)
Background: Peutz-Jeghers Syndrome (PJS) is a rare hereditary disease characterized by melanocytic macules of the lips
This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface
Immunogen: A synthesized peptide derived from human PAK3 around the phosphorylation site of Ser186
GPR82 Polyclonal Antibody - E-AB-91562 Size:60μL Mutations in this gene areGPR82 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 91562 60, E AB 91562 120, E AB 91562 200 Citations, Manuals and MSDS Available upon request. Abbreviation: GPR82 Target Synonym: GPR82 Research Areas: Signal Transduction Conjugation: Unconjugated Host: Rabbit Species Reactivity: Mouse, Rat Application: WB Isotype: IgG Clonality: Polyclonal UNIProt ID: Q96P67 Background: The protein encoded by this gene is an orphan G protein
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