Plasmid vector for in-vitro transcription of a dominant negative form of the mouse Trp53 (P53DD)
Clone info. | Plasmid vector for in-vitro transcription of a dominant negative form of the mouse Trp53 (P53DD) composed of 5' UTR of human hemoglobin subunit alpha (HBA), P53DD and 3' UTR of human hemoglobin subunit beta (HBB). |
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Vector backbone | phBG (plasmid) |
Selectable markers | Ampicillin, Kanamycin |
Gene/insert name | Mouse Trp53 cDNA Human HBA1 cDNA |
Depositor|Developer | Watanabe, Toshiaki | |
Sequence (full) ![]() |
RDB18331zzk01.seq provided by the depositor |
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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 obtained by use of the BIOLOGICAL RESOURCE, a citation of literature designated by the DEPOSITOR is requested. (Watanabe, T. et al., Genes Cells, 24(7): 473-484, 2019) |
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寄託者の指定する文献を引用する(Watanabe, T. et al., Genes Cells, 24(7): 473-484, 2019)。 |
Catalog # | Resource name | Availability | Shipping form | Fee (non-profit org.) |
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RDB18331 | phBG-p53DD | 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 phBG-p53DD was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB18331). |
Reference section:
Watanabe, T., Yamazaki, S., Yoneda, N., Shinohara, H., Tomioka, I., Higuchi, Y., Yagoto, M., Ema, M., Suemizu, H., Kawai, K., Sasaki, E., Highly efficient induction of primate iPS cells by combining RNA transfection and chemical compounds Genes Cells 24 (7): 473-484 (2019). PMID 31099158. [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 | Watanabe, T., Highly efficient induction of primate iPS cells by combining RNA transfection and chemical compounds Genes Cells 24 (7): 473-484 (2019). PMID 31099158. [link to RRC of NBRP] |
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