RAX2
retina and anterior neural fold homeobox 2
Sinónimos:
ARMD6, CORD11, QRX, RAXL1
Especie:
Human RAX2 (84839), Thale Cress RAX2 (818262), chicken RAX2 (373893), dog RAX2 (612000), domestic cat RAX2 (101098773), cow RAX2 (359713), sheep RAX2 (101117417)
ID UniProtKB:
ID del gen:
- Human(84839) Summary: 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. [provided by RefSeq, Jul 2008]
- Thale Cress(818262) transcription factor RAX2
- chicken(373893) retina and anterior neural fold homeobox 2
- dog(612000) retina and anterior neural fold homeobox 2
- domestic cat(101098773) retina and anterior neural fold homeobox 2
- cow(359713) retina and anterior neural fold homeobox 2
- sheep(101117417) retina and anterior neural fold homeobox 2
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Antibodies
Número de producto
Descripción
Reactividad de especies
Aplicación
Anti-RAX2 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
Reactividad de especies
human
Aplicación
immunohistochemistry