Mouse Anti-ENO1 Recombinant Antibody (clone 8H9G12) (CAT#: ZG-0250U)

Figure 1 Mouse Anti-ENO1 Antibody (ZG-0250U) in WB

Positive WB detected in: MCF-7 whole cell lysate, Hela whole cell lysate, Jurkat whole cell lysate, HepG2 whole cell lysate. All lanes ENO1 antibody at 1: 10000
Secondary
Goat polyclonal to mouse IgG at 1/10000 dilution
Predicted band size: 47 KDa
Observed band size: 47 KDa
Exposure time: 10s

Figure 2 Mouse Anti-ENO1 Antibody (ZG-0250U) in IHC

IHC image of ZG-0250U diluted at 1:500 and staining in paraffin-embedded human colon cancer 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 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.

Figure 3 Mouse Anti-ENO1 Antibody (ZG-0250U) in IF

Immunofluorescence staining of HepG2 cells with ZG-0250U at 1:130, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated Goat Anti-Mouse IgG(H+L).

Figure 4 Mouse Anti-ENO1 Antibody (ZG-0250U) in FC

Overlay histogram showing Hela cells stained with ZG-0250U (red line) at 1:260. 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 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of>10,000 events was performed.