RAX2 产品
(Retina and Anterior Neural Fold Homeobox 2 (RAX2))
Categories
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.
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Featured RAX2 Categories
Recommended RAX2 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN529792
Quantity
50 μg
Datasheet
Datasheet
Reactivity
Dog, Human
Application
WB
Validations
- (1)
Cat. No.
ABIN202046
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN1500622
Quantity
100 μL
Datasheet
Datasheet
Recommended RAX2 蛋白
Synonyms and alternative names related to RAX2
retina and anterior neural fold homeobox 2 S homeolog (rax2.S), retina and anterior neural fold homeobox 2 (RAX2), armd6, ARMD6, cord11, CORD11, qrx, QRX, raxl1, RAXL1, rx-lProtein level used designations for RAX2
- retina and anterior neural fold homeobox 2
- retinal homeobox-like transcription factor
- Q50-type retinal homeobox protein
- retina and anterior neural fold homeobox like 1
- retina and anterior neural fold homeobox protein 2
- retina and anterior neural fold homeobox-like protein 1
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