Fig. 3From: Protocol development for somatic embryogenesis, SSR markers and genetic modification of Stipagrostis pennata (Trin.) De WinterAgarose gel (3%) showing PCR amplification with the four SSR primers used for determining the genomic stability of the in vitro regenerated samples of Stipagrostis pennata (R1, R2, R3, R4). Seedlings of S. pennata from zygotic seed germination were used as controls (C1, C2, C3). DNA marker is indicated by MBack to article page