Application
Fig1: Blank control: A431.
Primary Antibody (green line): Rabbit Anti-ILDR1 antibody (ER1911-42)
Dilution: 1μg /10^6 cells;
Isotype Control Antibody (orange line): Rabbit IgG .
Secondary Antibody: Goat anti-rabbit IgG-AF647
Dilution: 1μg /test.
Protocol
The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 20% PBST for 20 min at room temperature. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at -20℃ .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
Application
Fig2: Sample:
DU145(Human) Cell Lysate at 30 ug
Primary: Anti-ILDR1 (ER1911-42) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 60 kD
Observed band size: 56 kD
Application
Fig3: Sample:
Prostate(Rat) Cell Lysate at 40 ug
Primary: Anti-ILDR1 (ER1911-42) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 60 kD
Observed band size: 56 kD
Application
Fig4: Sample:
Pancreas(Mouse) Cell Lysate at 40 ug
Primary: Anti-ILDR1 (ER1911-42) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 60 kD
Observed band size: 56kD