Skip to main content
. 2010 May 10;285(30):22999–23006. doi: 10.1074/jbc.M109.073783

FIGURE 1.

FIGURE 1.

DNA agarose gel (2.5%) showing process of high fidelity DNA shuffling of wild-type AtNHX1 gene. Lane M, DL2000, from top to the bottom: 2000, 1000, 750, 500, 250, and 100 bp. Lane 1, 1.6-kb fragment of AtNHX1 acquired by PCR; lane 2, DNA fragments after 2 min of DNaseI digestion in the presence of Mn2+, white box indicates the 100–200-bp fragments that are recycled; lane 3, fragment reassembly with Pfu polymerase; and lane 4, PCR amplification of the reassembly with Pfu polymerase.