黄金城集团

目录产品 » PE2max RNAase deletion

PEmax RNAase deletion

PEmax RNAase deletion involves modifications to the PEmax enzyme aimed at eliminating unwanted RNase activity, thus enhancing its stability and specificity. This advancement allows for more efficient target editing by minimizing the degradation of RNA components involved in the editing process, further improving the overall performance of the prime editing protocol.
RC00003
¥2800

联系黄金城集团
Description PEmax RNAase deletion involves modifications to the PEmax enzyme aimed at eliminating unwanted RNase activity, thus enhancing its stability and specificity. This advancement allows for more efficient target editing by minimizing the degradation of RNA components involved in the editing process, further improving the overall performance of the prime editing protocol.

single guide RNA (sgRNA) dependent single-stranded DNA cleavage

References David R Liu,et al.“Phage-assisted evolution and protein engineering yield compact, efficient prime editors”. Cell. 2023 Aug 31;186(18):3983-4002.e26.

Purity ≥90% by SDS-PAGE, 98% by SEC-HPLC
Residual DNase Non-specific DNase activity
Endotoxin Level Control <10EU/mg

Expression System Recombinant Cas9-based fusion with three NLS expressed by E.coli
Species S. pyogenes
Tag C-His tag
Molecular Weight 223.714KDa
Storage & Stability This product is supplied with storage buffer (50 mM Tris, 300 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 50% Glycerol pH7.5, at 25°C) and recommended to be stored at -80°C.

喜欢新升级的网站吗?

讨厌

不喜欢

一般

喜欢

非常喜欢

*