国产精品久久久久久永久牛牛,55国产福利在线视频,成人午夜精品视频在线观看

目錄產品 » GenCRISPR™/Cas9 基因編輯相關產品 » GenCRISPR™ Cas9 Enzymes » GenCrispr Cas9-N-NLS Nuclease
GenCrispr Cas9-N-NLS Nuclease

In vitro DNA cleavage assay with GenCrispr Cas9-N-NLS nuclease
Reactions were set up according to recommended conditions, and cleavage products were resolved on a 1% agarose gel. Input DNA is EcoRV-linearized pUC57 plasmid DNA

GenCrispr Cas9-N-NLS Nuclease

GenCrispr Cas9-N-NLS nuclease is the recombinant Streptococcus pyogenes Cas9 (wt) protein with a N-terminal nucleic localization signal (NLS) that can be used for genome editing by inducing site-specific DNA double stranded breaks. Cas9 protein forms a very stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component of the CRISPR/Cas9 system, which can localize to the nucleus immediately once entering the cell with the guide of the NLS. Compared with the mRNA or plasmid systems, transcription and translation processes are not required. This DNA-free system avoids the risk of inserting foreign DNA into the genome, which can be quite useful for gene editing-based disease therapy. Our highly pure and active Cas9 nuclease meets all of the researcher′s requirements (e.g. in vitro cleavage assay, RNP complex transfection, micro injection). Product Source: GenCrispr Cas9-N-NLS is produced by expression in an E. coli strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with a N-terminal nuclear localization signal (NLS). Key features: DNA-free: no external DNA added to system. High cleavage efficiency: NLS ensures the entry of Cas9 protein into nuclei. Low off target: transient expression of Cas9 nuclease. Time-saving: no need for transcription and translation. With this Cas9 Nuclease, you can: Screening the highly efficient and specific targeting gRNAs using in vitro DNA cleavage. In vivo gene editing combined with specific gRNA by electroporation or injection.
Z03388
詢價

聯系我們
Description

GenCrispr Cas9-N-NLS nuclease is the recombinant Streptococcus pyogenes Cas9 (wt) protein with a N-terminal nucleic localization signal (NLS) that can be used for genome editing by inducing site-specific DNA double stranded breaks. Cas9 protein forms a very stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component of the CRISPR/Cas9 system, which can localize to the nucleus immediately once entering the cell with the guide of the NLS. Compared with the mRNA or plasmid systems, transcription and translation processes are not required. This DNA-free system avoids the risk of inserting foreign DNA into the genome, which can be quite useful for gene editing-based disease therapy. Our highly pure and active Cas9 nuclease meets all of the researcher´s requirements (e.g. in vitro cleavage assay, RNP complex transfection, micro injection).

Product Source: GenCrispr Cas9-N-NLS is produced by expression in an E. coli strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with a N-terminal nuclear localization signal (NLS).

Key features:

  • DNA-free: no external DNA added to system.
  • High cleavage efficiency: NLS ensures the entry of Cas9 protein into nuclei.
  • Low off target: transient expression of Cas9 nuclease.
  • Time-saving: no need for transcription and translation.

With this Cas9 Nuclease, you can:

  1. Screening the highly efficient and specific targeting gRNAs using in vitro DNA cleavage.
  2. In vivo gene editing combined with specific gRNA by electroporation or injection.

Note

1000 nM is equal to 160 ng/ul.

Storage & Stability GenCrispr Cas9-N-NLS nuclease is supplied with 1 x storage buffer (10 mM Tris, 300 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 50% Glycerol pH7.4 at 25℃) and recommended to be stored at -20℃.

  • GenCrispr Cas9-N-NLS Nuclease
  • GenCrispr Cas9-N-NLS Nuclease

    In vitro DNA cleavage assay with GenCrispr Cas9-N-NLS nuclease
    Reactions were set up according to recommended conditions, and cleavage products were resolved on a 1% agarose gel. Input DNA is EcoRV-linearized pUC57 plasmid DNA


喜歡新升級的網站嗎?

討厭

不喜歡

一般

喜歡

非常喜歡

*
    主站蜘蛛池模板: 博罗县| 宜城市| 寿光市| 会昌县| 平舆县| 阿克苏市| 神农架林区| 永登县| 沅陵县| 凤阳县| 台州市| 河西区| 蕲春县| 广安市| 启东市| 西畴县| 霸州市| 太和县| 皋兰县| 扎赉特旗| 周宁县| 东源县| 班戈县| 扎兰屯市| 云和县| 南昌市| 东平县| 历史| 庆元县| 临泉县| 牡丹江市| 温泉县| 北流市| 宣恩县| 青州市| 苗栗县| 阳谷县| 洪雅县| 香河县| 辉南县| 柘荣县|