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. 2020 Nov 17;21(22):8665. doi: 10.3390/ijms21228665

Figure 7.

Figure 7

In vitro transcription of mouse EndoG (A) and mouse beta-actin (B) genes in plasmid constructs cleaved with recDNase I. mRNA expression was measured by real-time RT-PCR. Arbitrary units reflect coefficient of dilutions from 1:40 to 1:320 that were applied to the standard curve (n = 4). (C) Gel electrophoresis shows digestion of pET29b-mEndoG and pTRI-β-actin plasmids by recDNase I (Pulmozyme).