Rabbit Anti-TOP1 Recombinant Antibody (clone 6D8) (CAT#: ZG-0597U)

Figure 1 Rabbit Anti-TOP1 Antibody (ZG-0597U) in WB

Western Blot
Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, K562 whole cell lysate, HL60 whole cell lysate, PC-3 whole cell lysate
All lanes: TOP1 antibody at 1:2000
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 91 kDa
Observed band size: 91 kDa

Figure 2 Rabbit Anti-TOP1 Antibody (ZG-0597U) in IHC

IHC image of ZG-0597U diluted at 1:100 and staining in paraffin-embedded human small intestine 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.

Figure 3 Rabbit Anti-TOP1 Antibody (ZG-0597U) in IHC

IHC image of ZG-0597U diluted at 1:100 and staining in paraffin-embedded human colon cancer 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.

Figure 4 Rabbit Anti-TOP1 Antibody (ZG-0597U) in FC

Overlay histogram showing HepG2 cells stained with ZG-0597U (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followedby the antibody (1µg/1*106cells) for 1 h at 4°C.The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min at 4°C. Control antibody (green line) was Rabbit IgG (1µg/1*106cells) used under the same conditions. Acquisition of>10, 000 events was performed.

Figure 5 Rabbit Anti-TOP1 Antibody (ZG-0597U) in IP

Immunoprecipitating TOP1 in K562 whole cell lysate
Lane 1: Rabbit control IgG instead of ZG-0597U in K562 whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)
Lane 2: ZG-0597U(2µg)+ K562 whole cell lysate(500µg)
Lane 3: K562 whole cell lysate (10µg)