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  • GD111.JPG
GD111.JPG

DMT Enzyme


產品介紹

本產品為改良型的DpnI限制性內切酶,與傳統的DpnI限制性內切酶相比,具有更高的活性。該酶可以有效地識別并切割腺嘌呤甲基化的GmATC序列,而不能切割非甲基化的GATC序列。DMT Enzyme與多種PCR酶的反應緩沖液兼容(如EasyPfuTransStart FastPfu等),PCR結束后,在反應體系中直接加入該酶即可工作,反應結束后,無需加熱失活即可進行下游轉化實驗。    

產品組成

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References

1.Liu M , Feng Z , Ke H , et al. Tango1 spatially organizes ER exit sites to control ER export[J]. The Journal of Cell Biology, 2017, 216(4):1035-1049.

2.Bingqing L , Yingying Y , Yajie Z , et al. A Novel Enterovirus 71 (EV71) Virulence Determinant: The 69th Residue of 3C Protease Modulates Pathogenicity[J]. Frontiers in Cellular and Infection Microbiology, 2017, 7:26.

3.Wang T N , Zhao M . A simple strategy for extracellular production of CotA laccase in Escherichia coli, and decolorization of simulated textile effluent by recombinant laccase[J]. Applied Microbiology and Biotechnology, 2017, 101(2):685-696.