RAX2 Antikörper

Produktnummer ABIN7466343

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch RAX2 in WB. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für RAX2 Antikörper (ABIN7466343)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RAX2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-RAX2 Antikörper

Kreuzreaktivität: Human

Aufreinigung: Purified by antigen-affinity chromatography.

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

Isotyp: IgG

Anwendungsinformationen

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

Kommentare:

Positive Control: IMR32

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.86 mg/mL

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

Konservierungsmittel: Thimerosal (Merthiolate)

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu RAX2

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

Andere Bezeichnung: retina and anterior neural fold homeobox 2

Hintergrund: 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]

Molekulargewicht: 20 kDa

Gen-ID: 84839

UniProt: Q96IS3