RAX2 antibody

Catalog No. ABIN7466343

This Rabbit Polyclonal antibody specifically detects RAX2 in WB. It exhibits reactivity toward Human.

Quick Overview for RAX2 antibody (ABIN7466343)

Target: RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RAX2 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-RAX2 Antibody

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human RAX2. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: IMR32

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.86 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for RAX2

Target: RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))

Alternative Name: retina and anterior neural fold homeobox 2

Background: Retina and anterior neural fold homeobox 2 , ARMD6 , CORD11 , QRX , RAXL1,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]

Molecular Weight: 20 kDa

Gene ID: 84839

UniProt: Q96IS3