Fig. 2
From: An SPRI beads-based DNA purification strategy for flexibility and cost-effectiveness
Establishment and assessment of the SDPS method. A Workflow illustration of SPRI beads-based DNA extraction. B and C E-Gel visualization and recovery of DNA extracted using SDPS at different DNA size range markers. Control: AMPure XP beads, Input 1: 50 bp DNA marker (50 bp–800 bp, 2500 bp); Input 2: 1kbp DNA marker (250 bp-10 kb)；each group had four replicates, Mean ± SD. D and E Absorbing range and recovery of SDPS with different working ratio. Input: 50 bp DNA marker (50 bp–800 bp, 2500 bp); each group had two replicates, Mean ± SD. Figure 2B and D were cropped and the original gels are presented in Supplementary file 2 Fig. S2 and Fig. S3