If by "profile" you mean the conditions of the PCR reaction, then first determine the melting temperature (Tm) of your primers, either by running them through a program or by simply adding 4 °C for every G/C and 2 °C for every A/T. However, your primers do not look optimal from this point of view (they will have very differnt values of Tm, you will have to use a relatively low Tm in the program). Also, it is a good practice to have G or C at the 3' end as it improves annealing of the 3' end. With respect to elongation, check the data sheet accompanying the polymerase of your choice for specific instructions, but generally allow 30 sec/cycle for every 1 kb to be apmplified.