BUBR1 Kinase Antibody, IgG1, Clone: [8G1], Unconjugated, Mouse, Monoclonal Preis auf Anfrage

Artikelnummer: BYT-ORB344429
Artikelname: BUBR1 Kinase Antibody, IgG1, Clone: [8G1], Unconjugated, Mouse, Monoclonal Preis auf Anfrage
Artikelnummer: BYT-ORB344429
Hersteller Artikelnummer: orb344429
Alternativnummer: BYT-ORB344429-100
Hersteller: Biorbyt
Wirt: Mouse
Kategorie: Antikörper
Applikation: ELISA, IF, IP, WB
Spezies Reaktivität: Human
Immunogen: This protein A purified monoclonal antibody was produced by repeated immunizations with a recombinant protein corresponding to amino acid residues 1-350 of human BUBR1 Kinase protein.
Konjugation: Unconjugated
Alternative Synonym: mouse anti-BUBR1 antibody, Beta homolog of S. cerevisiae budding uninhibited by benzimidazoles antibody, BUB1 budding uninhibited by benzimidazoles 1 homolog beta antibody, Bub1A antibody, Mitotic checkpoint serine/threonine-protein kinase BUB1 beta, Mitotic checkpoint kinase MAD3L, MAD3/BUB1-related protein kinase, hBUBR1
BUBR1 Kinase Kinase antibody
Klonalität: Monoclonal
Konzentration: 1.0 mg/mL
Klon-Bezeichnung: [8G1]
Isotyp: IgG1
NCBI: 001202
UniProt: O60566
Puffer: Preservative: 0.01% (w/v) Sodium Azide. Stabilizer: None, Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Reinheit: This Protein A purified antibody is directed against human BUBR1 Kinase protein. The product was purified from tissue culture supernatant by chromatography. This antibody has only been tested on human cells. Reactivity against homologues from other sources is not known.
Formulierung: Liquid (sterile filtered)
Application Verdünnung: ELISA: 1:5,000 - 1:20,000, IF: 1:200 - 1:1,000, IP: 1:100, WB: 1:200 - 1:1,000
Anwendungsbeschreibung: Application Notes: This protein A purified antibody has been tested for use in immunoprecipitation, immunofluorescence staining and western blot and is capable of detecting endogenous protein. Specific conditions for reactivity should be optimized by the end user. Expect a predominant band at ~ 120 kDa corresponding to full-length protein by western blotting in the appropriate cell lysate or extract. Higher MW bands may be seen that may be due to hyper-phosphorylation of the protein. The use of HeLa whole cell lysates is recommended as a positive control. For IF microscopy use cells grown on cover slips fixed with 3.5% paraformaldehyde in PBS at pH 6.8. Permeabilize fixed cells with 0.2% Triton X-100 in 25 mM Tris Cl, pH 7.4 containing 0.1% BSA