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. 2017 Jun 30;11:54–65. doi: 10.2174/1874104501711010054

Table 2.

Western Blot Analysis. Protein samples concentration were adjusted with buffer (80%:20%, Laemmle buffer 5X: b-mercaptoethanol) to 3µg/mL. Antibodies were diluted with Tween OBB 0.1%, probed with goat anti-mouse, goat anti-rabbit (IR-Dye 670 or 800cw labeled secondary antisera, 1:15,000 dilution) in 0.1% Tween OBB for 1 h at room temperature. Washes were repeated three times in 1X PBS-T (0.1% Tween 20). Membranes images were obteined using LiCor Odyssey scanner. (NC= Negative control , PC = Positive control, Experimental NBQ-48 and ABQ-48 compounds.

Antibody NC PC NBQ-48 ABQ-48
Caspase 3 (1:1000) - + + +
Caspase 8 (0.3ugm/ml) - + - -
AIF (1:1000) - + - +