RS1 Antikörper (AA 34-224) (Fluoro647)

Produktnummer ABIN8031994

Der Fluoro647-konjugierte Kaninchen Polyklonal anti-RS1 Antikörper (ABIN8031994) detektiert spezifisch RS1 in FACS. Dieser Antikörper reagiert spezifisch mit Proben aus Human und Maus.

Kurzübersicht für RS1 Antikörper (AA 34-224) (Fluoro647) (ABIN8031994)

Target: RS1 (Retinoschisin 1 (RS1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RS1 Antikörper ist konjugiert mit Fluoro647

Applikation: Flow Cytometry (FACS)

Produktdetails anti-RS1 Antikörper (Fluoro647)

Bindungsspezifität: AA 34-224

Verwendungszweck: Anti-RS1 Antibody Fluoro647 Conjugated

Homologie: Human RS1 shares 96.9% amino acid (aa) sequence identity with mouse RS1.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human RS1 recombinant protein (Position: Y34-A224). Human RS1 shares 96.9% amino acid (aa) sequence identity with mouse RS1.

Isotyp: IgG

Anwendungsinformationen

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

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 RS1

Target: RS1 (Retinoschisin 1 (RS1))

Andere Bezeichnung: RS1

Hintergrund:

Background: Retinoschisin also known as X-linked juvenile retinoschisis protein is a lectin that in humans is encoded by the RS1 gene. This gene encodes an extracellular protein that plays a crucial role in the cellular organization of the retina. The encoded protein is assembled and secreted from photoreceptors and bipolar cells as a homo-oligomeric protein complex. Mutations in this gene are responsible for X-linked retinoschisis, a common, early-onset macular degeneration in males that results in a splitting of the inner layers of the retina and severe loss in vision.

Gene Full Name: retinoschisin 1

Gen-ID: 6247

UniProt: O15537