RAX2

BT-AP12236

Rabbit

IgG

20ul,50ul,100ul

Polyclonal

Synthesized peptide derived from human RAX2

The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

-20°C for 1 year

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.

Human: Q96IS3;

20240

Human: 84839

RAX2

Neuroscience; Epigenetics and nuclear signaling

RAX2