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ChEC-seq kinetics discriminates transcription factor binding sites by DNA sequence and shape in vivo.

Zentner GE, Kasinathan S, Xin B, Rohs R, Henikoff S
Nat Commun. 2015 Oct 22;6:8733. doi: 10.1038/ncomms9733. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
70231pGZ108 (pFA6a-3FLAG-MNase-kanMX6)ChEC-tagging vector encoding a short linker and aa 83-231 of Mnase in pFA6a-3HA-kanMX6 replacing the 3xHA tag. These vectors retain compatibility with the F2/R1 primer pairs commonly used for epitope
70232pGZ109 (pFA6a-3FLAG-MNase-HIS3MX6)ChEC-tagging vector encoding a 3xFLAG tag and aa 83-231 of Mnase in pFA6a-3HA- HIS3MX6 replacing the 3xHA tag. These vectors retain compatibility with the F2/R1 primer pairs commonly used for epitope
70233pGZ110 (pFA6a-3FLAG-MNase-TRP1)ChEC-tagging vector encoding a 3xFLAG tag and aa 83-231 of Mnase in pFA6a-3HA-Trp1 replacing the 3xHA tag. These vectors retain compatibility with the F2/R1 primer pairs commonly used for epitope tag
70234pGZ173 (pFA6a-SL-MNase-kanMX6)ChEC-tagging vector encoding a short linker and aa 83-231 of Mnase in pFA6a-3HA-kanMX6 replacing the 3xHA tag. These vectors retain compatibility with the F2/R1 primer pairs commonly used for epitope
72273pGZ136 (pRS406-pREB1-3FLAG-MNase-NLS)FLAG-Mnase expressed under the REB1 promoter

Antibodies from Article