RAX2 Antikörper (C-Term) (Cy3)

Produktnummer ABIN8031686

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch RAX2 in FACS. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für RAX2 Antikörper (C-Term) (Cy3) (ABIN8031686)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RAX2 Antikörper ist konjugiert mit Cy3

Applikation: Flow Cytometry (FACS)

Produktdetails anti-RAX2 Antikörper (Cy3)

Bindungsspezifität: C-Term

Verwendungszweck: Anti-RAX2 Antibody Cy3 Conjugated

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

Aufreinigung: Immunogen affinity purified.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, 1-3 μg/1x10⁶ cells

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

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

Haltbarkeit: 12 months

Details zu RAX2

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

Andere Bezeichnung: RAX2

Hintergrund:

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

Gen-ID: 84839

UniProt: Q96IS3