RAXL1 / RAX2

retina and anterior neural fold homeobox 2

RAXL1 / RAX2 is 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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Proteins (3)

Type

Over-Expression Lysate (2)

Recombinant (1)

Target

RAXL1 / RAX2 (3)

Publications

No (3)

Tag

GST (1)

Myc-DDK (Flag) (2)

Species

Human (2)

Source

293T Cells (1)

HEK 293 Cells (1)

Wheat Germ Extract (1)

Purification

Purified (1)

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Human RAXL1 / RAX2 Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G92269

Source:

293T Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

19.9 kDa

Price:

20 µg/$150

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Human RAXL1 / RAX2 Protein (Recombinant GST) (Full Length) - LS-G35835

Source:

Wheat Germ Extract

Tag:

GST

Molecular Weight:

46.5 kDa

Price:

2 µg/$439

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RAXL1 / RAX2 Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G108656

Source:

HEK 293 Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

19.9 kDa

Price:

100 µg/$494

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