RAX2 anticorps

N° du produit ABIN7466343

Cet anticorps Lapin Polyclonal détecte spécifiquement RAX2 dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour RAX2 anticorps (ABIN7466343)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RAX2 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-RAX2 anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

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

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: IMR32

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.86 mg/mL

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

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur RAX2

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

Autre désignation: retina and anterior neural fold homeobox 2

Sujet: 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]

Poids moléculaire: 20 kDa

ID gène: 84839

UniProt: Q96IS3