











Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.





Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.











参考图片
Sample:
1. A549 Cell (Human) Lysate at 40 ug
2. Hela Cell (Human) Lysate at 40 ug
3. Kidney (Mouse) Lysate at 40 ug
4. Heart (Mouse) Lysate at 40 ug
5. MCF-7 Cell (Human) Lysate at 40 ug
6. HL60 Cell (Human) Lysate at 40 ug
7. Ht1080 Cell (Human) Lysate at 40 ug
Primary: Anti- HIF-1 alpha (abs120168) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 92 kD
Observed band size: 120kD
Blank control (blue line): Hela (blue).
Primary antibody: Rabbit Anti- HIF-1 Alpha antibody
Dilution: 1μg /10^6 cells;
Isotype Control antibody: Rabbit IgG .
Secondary antibody: Goat anti-rabbit IgG-FITC
Dilution: 1μg /test.
Protocol
The cells were fixed with 80% methanol (5 min at -20℃) and then permeabilized with 0.1% PBS-Tween for 20 min at room temperature. Cells stained with Primary Antibody for 30 min at room temperature. The cells were then incubated in 1 X PBS/2%BSA/10% goat serum to block non-specific protein-protein interactions followed by the antibody for 15 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.