RAX2 antibody (C-Term)

Catalog No. ABIN8031695

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

Quick Overview for RAX2 antibody (C-Term) (ABIN8031695)

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), Immunohistochemistry (IHC)

Grade: Carrier-free

Product Details anti-RAX2 Antibody

Binding Specificity: C-Term

Purpose: Anti-RAX2 Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Characteristics: Anti-RAX2 Antibody. Tested in IHC, WB applications. This antibody reacts with Human.

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the C-terminus of human RAX2.

Isotype: IgG

Application Details

Application Notes: Western blot, 0.1-0.25 μg/mL, Human Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for RAX2

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

Alternative Name: RAX2

Background:

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.

Gene Full Name: retina and anterior neural fold homeobox 2

Molecular Weight: 18 kDa

Gene ID: 84839

UniProt: Q96IS3