Because of complex interactions among the components of PCR and the wi
de and increasing variety of applications in which this technique is u
sed, optimization is necessary for every reaction. Here we describe th
e use of experimental design techniques (2(k) fractional factorial des
ign and central composite design) to attain easier, quicker and cheape
r PCR optimization of DNA from blood spots. By determining the factors
affecting the product yield first (factors screening), the quantity o
f template DNA needed for PCR and the Mg2+ concentration are easily op
timized (factors optimization).