RAX2 antibody (C-Term) (FITC)

Catalog No. ABIN8031690

The Rabbit Polyclonal anti-RAX2 antibody is suitable to detect RAX2 in samples from Human. It has been validated for FACS.

Quick Overview for RAX2 antibody (C-Term) (FITC) (ABIN8031690)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RAX2 antibody is conjugated to FITC

Application: Flow Cytometry (FACS)

Product Details anti-RAX2 Antibody (FITC)

Binding Specificity: C-Term

Purpose: Anti-RAX2 Antibody FITC Conjugated

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

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: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

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

Gene ID: 84839

UniProt: Q96IS3