We introduce a model system consisting of self-assembled polyamide anisotropic colloids suspended in all aqueous surfactant solution for studies of the dynamics of rod networks, gels, and glasses. The colloidal particles are formed by recrystallization of a polyamide from an aqueous surfactant phase at temperatures front 59 to 100 degrees C. The aspect ratio increases monotonically with temperature from T = 59 degrees C to T = 100 degrees C and rods with all aspect ratio r = 8 +/-1 to r = 306 +/- 14 form. We show by confocal laser scanning microscopy and dynamic light scattering a structural transition front dilute rod behavior with diffusive dynamics to a homogeneous network structure with increasingly slow dynamics as the volume fraction is increased. Furthermore, increasing the aspect ratio of rods induces a similar structural transition from dilute rod behavior to a network structure, although at a lower volume fraction. Finally, we vary the pair potential between the rods by a polymer-induced depletion interaction and thereby observe all unexpected network-to-bundle transition. The bundles are several rod diameters wide and 1-2 rod lengths long. The rods appear to be ordered nematically within each bundle. The bundling transition leads to an order of magnitude decrease in the storage modulus of the Suspensions. The results call be applied to develop strategies for complex fluid Stabilization as well as for fundamental studies of rod gelation and vitrification.