DLL3 Antikörper (AA 510-590)

Produktnummer ABIN7228240

Der Kaninchen Polyklonal Anti-DLL3 Antikörper wurde für WB und ELISA validiert. Er ist geeignet, DLL3 in Proben von Human, Maus und Ratte zu detektieren.

Kurzübersicht für DLL3 Antikörper (AA 510-590) (ABIN7228240)

Target: DLL3 (delta Like Protein 3 (DLL3))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DLL3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-DLL3 Antikörper

Bindungsspezifität: AA 510-590

Verwendungszweck: DLL3 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of DLL3 protein

Aufreinigung: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human DLL3 protein at AA range: 510-590

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Kommentare:

Primary Antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Details zu DLL3

Target: DLL3 (delta Like Protein 3 (DLL3))

Andere Bezeichnung: DLL3

Hintergrund: Rabbit Anti-DLL3 Polyclonal Antibody,Delta-like protein 3, Drosophila Delta homolog 3, Delta3,DLL3 encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in DLL3 cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for DLL3.,DLL3

Molekulargewicht: observerd band 67kDa

Gen-ID: 10683

UniProt: Q9NYJ7

Pathways: Notch Signalweg