Expression vector of sgRNA for targeting mouse Gli3-exon2.
Clone info. | Expression vector of sgRNA for targeting mouse Gli3-exon2, SpCAS9 and 2A-Puro, see Fig1B of Makino, S. et al. Sci. Rep., 6: 39608, 2016. |
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Comment | Expression was confirmed by the depositor with direct sequencing and western blotting. Recommended host, Stbl3. |
Vector backbone | pSpCas9(BB)-2A-Puro (PX459) (plasmid) |
Selectable markers | Amp^r (E. coli), Puro^r (mammalian cells). |
Gene/insert name | mouse Gli3 genomic |
Depositor|Developer | Gondo, Yoichi | Makino, Shigeru | |
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 ![]() ![]() ![]() Exclusive MTA (For the DNA materials containing CRISPR/Cas9 technologies and for not-for-profit academic purpose) [Word ![]() Please visit Information of Request for Distribution.[link] |
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Terms and conditions for distribution | In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature designated by the DEPOSITOR is requested (Makino,S. et al. Sci. Rep., 6: 39608, 2016). Additional terms and conditions: The use of the BIOLOGICAL RESOURCE is restricted to the academic researches conducted by non-profit organization. |
Remarks | The BIOLOGICAL RESOURCE contains CRISPR/Cas9 technologies and is not provided to for-profit organization or for for-profit research by non-profit organizations. |
必要書類 | 提供依頼書 ![]() ![]() 専用MTA(CRISPR/Cas9内包遺伝子材料専用 非営利学術目的)をお使いください [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。 |
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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寄託者の指定する文献を引用する (Makino,S. et al. Sci. Rep., 6: 39608, 2016)。 MTAに書く付加的使用条件: 本件リソースの使用は学術機関での学術研究に限る。 |
備考 | 本件リソースはCRISPR/Cas9 technologyを用いたゲノム編集バイオリソースです。営利機関および非営利機関による営利目的研究には提供いたしません。 |
Catalog # | Resource name | Availability | Shipping form | Fee (non-profit org.) |
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RDB15037 | pSpCas9-mGli3-exon2_sgRNA | Under QC test. Please contact us. | DNA solution |
JPY 9,460 (not-for-profit academic purpose) plus cost of shipping containers, dry ice (if required) and shipping charge |
Materials & Methods section:
The pSpCas9-mGli3-exon2_sgRNA was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB15037). |
Reference section:
Makino, S., Fukumura, R., Gondo ,Y., Illegitimate translation causes unexpected gene expression from on-target out-of-frame alleles created by CRISPR-Cas9. Sci. Rep. 6: 39608 (2016). PMID 28000783. [link to RRC of NBRP] |
Further references such as user reports and related articles (go to bottom)
Please wait for results of QC test to be uploaded. This clone will be sequenced a portion for examination.
Original, user report and related articles
original | Makino, S., Illegitimate translation causes unexpected gene expression from on-target out-of-frame alleles created by CRISPR-Cas9. Sci. Rep. 6: 39608 (2016). PMID 28000783. [link to RRC of NBRP] |
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