CCDC11 Antikörper (AA 330-380) (AbBy Fluor® 594)

Produktnummer ABIN2811194

Dieses Anti-CCDC11-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von CCDC11 in WB, IF (cc) und IF (p). Geeignet für Human und Maus.

Kurzübersicht für CCDC11 Antikörper (AA 330-380) (AbBy Fluor® 594) (ABIN2811194)

Target: CCDC11 (Coiled-Coil Domain Containing 11 (CCDC11))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC11 Antikörper ist konjugiert mit AbBy Fluor® 594

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-CCDC11 Antikörper (AbBy Fluor® 594)

Bindungsspezifität: AA 330-380

Spezifität: Due to the similarity of this protein to RWD domain-containing protein 1, there is a chance that this antibody will react with this protein based on a 75 % non-sequential amino acid similarity.

Kreuzreaktivität: Human, Maus, Ratte

Homologie: Cow,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC11

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu CCDC11

Target: CCDC11 (Coiled-Coil Domain Containing 11 (CCDC11))

Andere Bezeichnung: CCDC11

Hintergrund:

Synonyms: HTX6, CCDC11, Coiled-coil domain-containing protein 11

Background: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.

Gen-ID: 220136

UniProt: Q96M91