GPR143 Rabbit anti-Human, Polyclonal, Invitrogen
Rabbit Polyclonal Antibody
Manufacturer: Invitrogen OSR00146W
Reconstitute with 100 µL of distilled water. Centrifuge to remove any insoluble material.Ocular albinism type 1 protein is a conserved integral membrane protein with seven transmembrane domains. It is expressed in the eye and epidermal melanocytes. Defects in GPR143 are the cause of ocular albinism type 1 (OA1); also known as Nettleship-Falls type ocular albinism. OA1 is an X-linked disorder characterized by severe impairment of visual acuity, retinal hypopigmentation and the presence of macromelanosomes.
|whole serum with no preservative|
|G-protein coupled receptor 143, ocular albinism type 1 protein, GPR143, OA1|
|Immunohistochemistry, Western Blot|
|A synthetic peptide from the 3d cytoplasmic domain of human GPR143 (OA1) conjugated to an immunogenic carrier protein was used as the antigen|
|Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.|
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