RAX2 Rabbit Polyclonal Antibody

This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6| an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch' s membrane. Defects in this gene can also cause cone-rod dystrophy type 11| a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity| followed by the degeneration of rod photoreceptor cells| which progresses to night blindness and the loss of peripheral vision. Alternative splicing results in multiple transcript variants.

1 mg/ml

20240