“…We used a total of 12 microsatellite markers (nSSRs: Kp05, Kp15, Kp27, Kp28, Kp36, Kp42, Kp48, Kp49, Kp51, Kp65, Kp69, Kp74) developed specifically for K. palmata by Sun et al (2010). Primers were labeled with a fluorescent dye, either HEX or 6‐FAM (Applied Biosystems, Foster City, California, USA), and PCR amplifications were performed on a GeneAmp 9700 DNA Thermal Cycler (Perkin‐Elmer, Waltham, Massachusetts, USA) using protocols described by Sun et al (2010). PCR products were separated on a MegaBACE 1000 (GE Healthcare Biosciences, Pittsburgh, PA, USA).…”