Microsatellite PCRs were performed in MJ DNA Engine
Tetrad machines using the protocol outlined in Wilson
(2006a). PCRs were diluted into a single plate for genotyping.
Multiplexed reactions were diluted 1:10 and individual
PCRs were diluted 1:20. One microlitre of the bulk PCR
dilutions was added to a plate containing 0.09
μ
L of the
genescan
500 LIZ genotyping standard and 9.91
μ
L of