C21orf58 Antikörper (Cy3)

Produktnummer ABIN1423607

Der Kaninchen Polyklonal Anti-C21orf58-Antikörper wurde für WB und IF (p) validiert. Er ist geeignet, C21orf58 in Proben von Human, Maus und Ratte zu detektieren.

Kurzübersicht für C21orf58 Antikörper (Cy3) (ABIN1423607)

Target: C21orf58 (Chromosome 21 Open Reading Frame 58 (C21orf58))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C21orf58 Antikörper ist konjugiert mit Cy3

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

Produktdetails anti-C21orf58 Antikörper (Cy3)

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21orf58

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 C21orf58

Target: C21orf58 (Chromosome 21 Open Reading Frame 58 (C21orf58))

Andere Bezeichnung: C21orf58

Hintergrund:

Synonyms: C21orf58, Chromosome 21 open reading frame 58, CU058_HUMAN, Hypothetical protein LOC54058, Uncharacterized protein C21orf58.

Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf58 gene product has been provisionally designated C21orf58 pending further characterization.

Gen-ID: 54058