C20orf166 Antikörper (AA 21-117) (Biotin)

Produktnummer ABIN1699890

Produktdetails anti-C20orf166 Antikörper (Biotin)

Target: C20orf166 (Chromosome 20 Open Reading Frame 166 (C20orf166))

Bindungsspezifität: AA 21-117

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C20orf166 Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf166

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Haltbarkeit: 12 months

Details zu C20orf166

Target: C20orf166 (Chromosome 20 Open Reading Frame 166 (C20orf166))

Andere Bezeichnung: C20orf166 (C20orf166 Produkte)

Synonyme: dJ353C17.1 antikoerper, MIR1-1 host gene antikoerper, MIR1-1HG antikoerper

Hintergrund:

Synonyms: C20orf166, Chromosome 20 open reading frame 166, CT166_HUMAN, dJ353C17.1, RP3-353C17.2, Uncharacterized protein C20orf166.

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf166 gene product has been provisionally designated C20orf166 pending further characterization.

Gen-ID: 128826