Expression vector of human TERT
Alternative name | clone 2 |
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Clone info. | Expression vector for human TERT and DsRed2. EcoRI-SalI fragment was derived from pCDNA3-hTERTn2. |
Vector backbone | pIRES2-DsRed2 (Plasmid) |
Size of vector backbone | 5.3 kb |
Selectable markers | Kan^r (E. coli), Neo^r (mammalian cell) |
Gene/insert name | Human TERT cDNA |
Depositor|Developer | Yokoyama, Kazunari | |
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 ![]() ![]() ![]() In order to receive this biological resource, please request the Exclusive MTA to us. 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 | Manuscripts for the publication shall be made through the discussion between Depositor and Recipient Investigator. |
Remarks | An additional license fee for DNA resources containing fluorescent proteins owned by, or licensed to, Clontech Laboratories, Inc. is required. |
必要書類 | 提供依頼書 ![]() ![]() 本件遺伝子材料の依頼に際し、専用MTA(英語版のみ)の提出をお願いします。当室にご請求ください。 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 | 使用にあたっては常に密な連絡をとり、発表等に関しても事前に合意を要する。 |
備考 | クロンテック社の蛍光タンパク質 (DsRed2、mCherry)を含むクローン。ライセンス料相当額を負担して頂きます。 |
Catalog # | Resource name | Availability | Shipping form | Fee (non-profit org.) |
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RDB03442 | phTERT_i_DsRed2 | 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 plus licensing fee equivalent for fluorescent protein |
Materials & Methods section:
The phTERT_i_DsRed2 was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB03442). |
Reference section:
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
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