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Ocular Albinism 1 antibodyRabbit Polyclonal anti-Ocular Albinism 1
Ocular albinism 1 (Nettleship-Falls; OA1) is an Orphan-U GPCR with an unknown ligand. Ocular albinism type 1 (OA1) is an inherited disorder characterized by severe reduction of visual acuity, photophobia, and retinal hypopigmentation. Ocular albinism type 1 protein is a conserved integral membrane protein with seven transmembrane domains. Misfolding of the OA1 protein has been suggested as a major pathogenic mechanism in OA1. OA1 protein expression has been documented in the eye and in epidermal melanocytes.Alternate Names: anti-ALBINISM OCULAR TYPE I antibody, anti-G protein coupled receptor 143 antibody, anti-GPR143 antibody, anti-MOA1 antibody, anti-NETTLESHIP FALLS TYPE OCULAR ALBINISM antibody, anti-OA1 antibody, anti-Ocular albinism type 1 protein antibody, anti-Ocular albinism type 1 protein homolog antibody, anti-Ocular albinism1 Nettleship-Falls type antibodyHost: RabbitResearch Areas: GPCR (G Protein-Coupled Receptor), IHC GradeImmunogen: Synthetic peptide [KLH conjugated] made to the N-term extracellularEpitope: N-terminal extracellular domain of humanSpecies Reactivity: Human. 45% identity and homology with mouse. |
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Ocular Albinism 1 (Nettleship Falls; OA1) detection using NLS 2123 on human eye (retina).
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