C20ORF196 Antikörper (AbBy Fluor® 647)

Produktnummer ABIN1404162

Produktdetails anti-C20ORF196 Antikörper (AbBy Fluor® 647)

Target: C20ORF196 (Chromosome 20 Open Reading Frame 196 (C20ORF196))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C20ORF196 Antikörper ist konjugiert mit AbBy Fluor® 647

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf196

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 C20ORF196

Target: C20ORF196 (Chromosome 20 Open Reading Frame 196 (C20ORF196))

Andere Bezeichnung: C20orf196 (C20ORF196 Produkte)

Synonyme: chromosome 20 open reading frame 196 antikoerper, C20orf196 antikoerper

Hintergrund:

Synonyms: C20orf196, CT196_HUMAN, Uncharacterized protein C20orf196, SHLD1_HUMAN, Shieldin complex subunit 1, SHLD1.

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 C20orf196 gene product has been provisionally designated C20orf196 pending further characterization.

Gen-ID: 149840