If you are detecting your protein with an HRP-conjugated antibody (in an ELISA for instance), you can easily develop it with TMB substrate (turns positive wells blue), and stop the reaction with 1M H2SO4 (turns positive wells yellow), then read absorbance on a plate reader. If you are using a capturing antibody, make sure there isn't cross-reactivity between the HRP-conjguated antibody used for detection, and the capturing antibody however. For westerns, I like the Lumiglo substrate. It's very easy to mix/use from my experience. Good luck!