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Ehssp1 homologue in E. dispar. (A) PCR amplification of E. dispar genomic DNA using ABR-F-ABR-R primers. The PCR product was electrophoresed in 1.2% agarose gel at 4 V/cm. (B) The PCR product in (A) was cloned in pGEMT-Easy vector. Clones were randomly picked and the inserts released by digesting with Eco RI. The digests were electrophoresed on a 1.2% agarose gel. The portion of the ethidium bromide-stained gel containing the inserts is shown.
