RAD51C Antikörper

Produktnummer ABIN7262879

Produktdetails anti-RAD51C Antikörper

Target: RAD51C (DNA Repair Protein RAD51 Homolog 3 (RAD51C))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RAD51C Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human RAD51C (NP_002867.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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. Avoid freeze / thaw cycles.

Details zu RAD51C

Target: RAD51C (DNA Repair Protein RAD51 Homolog 3 (RAD51C))

Andere Bezeichnung: RAD51C (RAD51C Produkte)

Synonyme: RGD1563765 antikoerper, CG2412 antikoerper, Dm CG2412 antikoerper, Dmel\\CG2412 antikoerper, zgc:101596 antikoerper, RAD51C antikoerper, Rad51c antikoerper, ATRAD51C antikoerper, F4L23.21 antikoerper, RAS associated with diabetes protein 51C antikoerper, R51H3 antikoerper, Rad51l2 antikoerper, BROVCA3 antikoerper, FANCO antikoerper, RAD51L2 antikoerper, RAD51 paralog C antikoerper, Rad51 recombinase D antikoerper, Rad51 DNA recombinase 3 antikoerper, RAD51C protein antikoerper, RAD51 homolog C antikoerper, RAS associated with diabetes protein 51C antikoerper, RAD51C antikoerper, Rad51c antikoerper, Rad51D antikoerper, rad51c antikoerper

Hintergrund: This gene is a member of the RAD51 family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51 and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with other RAD51 paralogs and is reported to be important for Holliday junction resolution. Mutations in this gene are associated with Fanconi anemia-like syndrome. This gene is one of four localized to a region of chromosome 17q23 where amplification occurs frequently in breast tumors. Overexpression of the four genes during amplification has been observed and suggests a possible role in tumor progression. Alternative splicing results in multiple transcript variants.

Gen-ID: 5889

UniProt: O43502

Pathways: DNA Reparatur