Background:

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.

Classification:

Primary antibody

Alternative names:

RAX2

Species reactivity:

Human, Rat, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human RAX2

Concentration:

1 mg/ml

Molecular weight:

20240

Applications:

WB

Storage:

-20°C for 1 year

More info:

Email: info@sobekbio.com

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