OA1/GPR143 Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody

Supplier:  Bioss BS11791R

Catalog No. 50-198-1671

Description

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.

Specifications

• Antigen: OA1/GPR143
• Classification: Polyclonal
• Conjugate: Unconjugated
• Gene: GPR143
• Gene Alias: G protein-coupled receptor 143; GPR143; G-protein coupled receptor 143; homolog of human ocular albinism 1 (Nettleship-Falls); MOA1; NYS6; OA1; ocular albinism 1; Ocular albinism type 1 protein; Ocular albinism type 1 protein homolog; RGD1565799
• Host Species: Rabbit
• Purification Method: Protein A
• Regulatory Status: RUO
• Gene ID (Entrez): 4935
• Content And Storage: -20°C
• Form: Liquid

• Applications: Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
• Concentration: 1 μg/mL
• Formulation: PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
• Gene Accession No.: P51810
• Gene Symbols: GPR143
• Immunogen: KLH conjugated synthetic peptide derived from human OA1.
• Quantity: 100 μL
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgG