Nucleic Acids Research
Home Corrigendum to article “A programmable omnipotent Argonaute nuclease from mesophilic bacteria Kurthia massiliensis’’
Corrigendum to article “A programmable omnipotent Argonaute nuclease from mesophilic bacteria <i>Kurthia massiliensis</i>’’
Corrigendum to article “A programmable omnipotent Argonaute nuclease from mesophilic bacteria Kurthia massiliensis’’

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Liu,Li,Jiang,Wang,Zhang,Liu,He,Chen,Yang,Wang,Wang,and Ma: Corrigendum to article “A programmable omnipotent Argonaute nuclease from mesophilic bacteria Kurthia massiliensis’’

Nucleic Acids Research, Volume 49, Issue 3, 22 February 2021, Pages 1597–1608, https://doi.org/10.1093/nar/gkaa1278

In Figure 3 the lower-left panel should be labelled as B, and the upper-right panel should be labelled as C.

This correction does not affect the results, discussion and conclusions presented in the article. The published article has been updated.

Effects of the guide length on KmAgo activity. (A) Effects of the 5′P-gDNA length on DNA cleavage activity. (B) Effects of the 5′P-gDNA length on RNA cleavage activity. (C) Effects of the 5′P-gRNA length on RNA cleavage activity. (D) Effects of the 5′P-gRNA length on DNA cleavage activity. Black triangle indicates the 30 nt 5′P-gRNA. All experiments were performed at the 4:2:1 KmAgo:guide:target molar ratio in reaction buffer containing Mn2+ ions for 15 min at 37°C.
Figure 3.

Effects of the guide length on KmAgo activity. (A) Effects of the 5′P-gDNA length on DNA cleavage activity. (B) Effects of the 5′P-gDNA length on RNA cleavage activity. (C) Effects of the 5′P-gRNA length on RNA cleavage activity. (D) Effects of the 5′P-gRNA length on DNA cleavage activity. Black triangle indicates the 30 nt 5′P-gRNA. All experiments were performed at the 4:2:1 KmAgo:guide:target molar ratio in reaction buffer containing Mn2+ ions for 15 min at 37°C.