Skip to main content
Figure 1 | BMC Genomics

Figure 1

From: A new genomic tool, ultra-frequently cleaving TaqII/sinefungin endonuclease with a combined 2.9-bp recognition site, applied to the construction of horse DNA libraries

Figure 1

PCR fragment DNA substrates. Putative recognition sequence of TaqII is in bold and underlined. Arrows mark the cleavage. The restriction fragments lacking TaqII recognition sequence are in italics. (A) PCR fragment without a TaqII site. (B) PCR DNA fragment with a single 5′-GACCGA-3′ site.

Back to article page

BMC Genomics

ISSN: 1471-2164

Contact us