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EJNMMI Radiopharmacy and Chemistry
Fig. 3 | EJNMMI Radiopharmacy and Chemistry

Fig. 3

From: Effect of the versatile bifunctional chelator AAZTA5 on the radiometal labelling properties and the in vitro performance of a gastrin releasing peptide receptor antagonist

Fig. 3

Saturation binding study on intact PC3 cells, using increasing concentrations of 68/natGa-LF1, 177/natLu-LF1, 111/natLF-LF1 and 177/natLu-RM2, ranging from 1 to 100 nM. Dissociation constant (Kd) and maximum number of binding sites (Bmax) were calculated from nonlinear regression analysis using GraphPad Prism

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