| Identifiers | ||
| Product Name | Ocular Albinism 1 (OA1/GPR143) | |
| Catalogue No. | CM525935 | |
| Description | 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. | |
| Host | Rabbit | |
| Storage Condition | Long term: -70°C; Short term: -4°C | |
| Brand | Packing | Pricing | Quote request |
| IL | 50 ul | Inquiry | Ask Quote |
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