| Application | Recommended Dilution |
|---|---|
| WB | 1:1000-1:5000 |
| IF | 1:50-1:200 |
| IP | 1:200-1:2000 |
Immunofluorescence staining of Hela cells with CSB-PA13457A0Rb at 1:66, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
Western Blot
Positive WB detected in: PC-3 whole cell lysate, K562 whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate
All lanes: ANXA1 antibody at 2µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 39 kDa
Observed band size: 39 kDa
Immunoprecipitating ANXA1 in K562 whole cell lysate
Lane 1: Rabbit control IgG instead of CSB-PA13457A0Rb in K562 whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)
Lane 2: CSB-PA13457A0Rb (8µg) + K562 whole cell lysate (500µg)
Lane 3: K562 whole cell lysate (10µg)
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