BUB1 Antibody, IgG1, Clone: [14H5], Unconjugated, Mouse, Monoclonal Preis auf Anfrage

Artikelnummer: BYT-ORB344427
Artikelname: BUB1 Antibody, IgG1, Clone: [14H5], Unconjugated, Mouse, Monoclonal Preis auf Anfrage
Artikelnummer: BYT-ORB344427
Hersteller Artikelnummer: orb344427
Alternativnummer: BYT-ORB344427-100
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 281-419 of human BUB1 protein.
Konjugation: Unconjugated
Alternative Synonym: mouse anti-BUB1 antibody, Budding uninhibited by benzimidazoles 1 homolog antibody, hBUB1 antibody, Mitotic checkpoint serine/threonine protein kinase BUB1 antibody
BUB1 antibody
Klonalität: Monoclonal
Konzentration: 1.0 mg/mL
Klon-Bezeichnung: [14H5]
Isotyp: IgG1
NCBI: 004327
UniProt: O43683
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 BUB1 protein. The product was purified from tissue culture supernatant by chromatography. This antibody reacts with BUB1 from human cells. No reactivity is seen for homologues from Xenopus or Kangaroo Rat. Reactivity against homologues from other sources is not known.
Formulierung: Liquid (sterile filtered)
Application Verdünnung: ELISA: 1:5,000 - 1:20,000, IF: 1:500 - 1:2,000, IP: 1:200, WB: 1:500 - 1:2,000
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 ~ 160 kDa corresponding to full-length protein by western blotting in the appropriate cell lysate or extract. The use of HeLa whole cell lysates prepared using a RIPA buffer 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 OR 100% methanol at -20 C. Permeabilize fixed cells with 0.5% Triton X-100