ANKS3 Antikörper (FITC)

Produktnummer ABIN1400828

Der Kaninchen Polyklonal Anti-ANKS3-Antikörper wurde für IF (p) validiert. Er ist geeignet, ANKS3 in Proben von Human, Maus und Ratte zu detektieren.

Kurzübersicht für ANKS3 Antikörper (FITC) (ABIN1400828)

Target: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ANKS3 Antikörper ist konjugiert mit FITC

Applikation: Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-ANKS3 Antikörper (FITC)

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human ANKS3

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: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: 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 ANKS3

Target: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Andere Bezeichnung: ANKS3

Hintergrund:

Synonyms: Ankyrin repeat and SAM domain containing protein 3, Ankyrin repeat and sterile alpha mot domain containing 3, KIAA1977, ANKS3_HUMAN.

Background: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Gen-ID: 124401