CD19 Monoclonal Antibody, IgG2b, Clone: [4C6G1], Unconjugated, Mouse

Artikelnummer: CSB-MA004888A1M
Artikelname: CD19 Monoclonal Antibody, IgG2b, Clone: [4C6G1], Unconjugated, Mouse
Artikelnummer: CSB-MA004888A1M
Hersteller Artikelnummer: CSB-MA004888A1m
Alternativnummer: CSB-MA004888A1M-100UL, CSB-MA004888A1M-50UL
Hersteller: Cusabio
Wirt: Mouse
Kategorie: Antikörper
Applikation: ELISA, FC, IHC, WB
Spezies Reaktivität: Human
Konjugation: Unconjugated
Alternative Synonym: B-lymphocyte antigen CD19, B-lymphocyte surface antigen B4, Differentiation antigen CD19, T-cell surface antigen Leu-12, CD19, CD19
Klonalität: Monoclonal
Klon-Bezeichnung: [4C6G1]
Isotyp: IgG2b
UniProt: P15391
Puffer: Preservative: 0.03% Proclin 300<br />Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Reinheit: >95%, Protein A purified
Formulierung: Liquid
Target-Kategorie: CD19
Application Verdünnung: Recommended dilution: WB:1:1000-1:5000, IHC:1:50-1:200
Overlay histogram showing Raji cells stained with CSB-MA004888A1m (red line) at 1:50. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
IHC image of CSB-MA004888A1m diluted at 1:100 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image of CSB-MA004888A1m diluted at 1:100 and staining in paraffin-embedded human spleen tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
Western Blot
Positive WB detected in: Raji whole cell lysate
All lanes: CD19 antibody at 1:2000
Secondary
Goat polyclonal to Mouse IgG at 1/10000 dilution
Predicted band size: 61 kDa
Observed band size: 95 kDa