Selection plasmid for the positive clone of CRISPR/Cas9 system in the culture cells.
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| Clone info. | Selection plasmid for the positive clone of CRISPR/Cas9 system in the culture cells. For the selection of sgRNA on double-strand breaks by Neomycin (or G418) resistance. MCS: BamHI, NheI, PstI, SalI, EcoRI, and EcoRV. This construct was created based on the pCAG-EGxxFP (Mashiko, O., Sci. Rep. 3: 3355, 2013). |
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| Vector backbone | pCAGGS (Plasmid) |
| Selectable markers | Amp^r |
| Growth conditions | 37oC, LB + Amp. |
| Depositor|Developer | Hashido, Kazuo | Terumitsu, Mika | |
Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
| Ordering forms | Order form [Credit Card Payment MTA, for use for not-for-profit academic purpose [Word Please visit Information of Request for Distribution.[link] For for-profit-research purpose, please contact us. |
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| Terms and conditions for distribution | In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, description of “This construct was created based on the pCAG-EGxxFP (Mashiko, O., Sci. Rep. 3: 3355, 2013)” is requested. |
[open/close]| 必要書類 | 提供依頼書 提供同意書 (MTA, 非営利学術目的用)[Word 手続きの概要は、「提供申込みについて[link]」をご覧ください。営利目的利用についてはお問い合わせください。 |
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| MTAに書く使用条件 | 利用者は、研究成果の公表にあたって謝辞の表明を必要とする。利用者は研究成果の公表に当たって、本件リソースがpCAG-EGxxFP (Mashiko, O.,Sci. Rep. 3: 3355, 2013) を基に作成したことを記すこと。 |
| Catalog # | Resource name | Shipping form | Fee |
|---|---|---|---|
| RDB16803 | pCAG-NexxoR | DNA solution |
Materials & Methods section:
| The pCAG-NexxoR was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB16803). |
Reference section:
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