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. 2024 Nov 28;2024:5394494. doi: 10.1155/adpp/5394494

Figure 1.

Figure 1

Far Western Blotting of recombinant TcCaNB with membrane proteins from B16-F10, HeLa, and Vero cells. 100 μg of membrane proteins from B16-F10 and HeLa cells and 30 μg of recombinant TcCaNB were used. The interaction was detected with anti-TcCaNB and anti-h/m/r CANB antibodies. (a) Far WB using anti-TcCaNB antibody for detection. (b) WB control using anti-TcCaNB antibody. (c) Far WB using anti-h/m/r CaNB antibody. (d) WB control using anti-h/m/r CaNB antibody. (e) Far WB using anti-h/m/r CaNB antibody. (f) WB control using anti-h/m/r CaNB antibody. 10 μg of BSA was used as negative control in Far WB. 100 μg of B16-F10, HeLa, and Vero membrane proteins was used in WB controls.