Recombinant adenovirus harboring enhanced green fluorescent protein cDNA
|Resource name||AxCALNLEGFP (forward)|
|Clone info.||Enhanced green fluorescent protein (EGFP) is cloned into the SwaI site of pAxCALNLw. (Direction:forward). Replication-competent adenovirus has not been detected by PCR.
Expression of proteins was not determined at the production of this virus.
|Vector backbone||pAxCALNLw (Adenovirus)|
|Gene/insert name||Aequorea victoria GFP cDNA|
|Depositor||DNA Bank, ||
Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
|Terms and conditions set forth by the DEPOSITOR||1. The RECIPIENT agrees to use the BIOLOGICAL RESOURCE only for academic research in the non-profit organization. 2. In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested.|
|Remarks||((Additional form)) CAG(FormE)|
Please use Schedule A (GFP-A) additionally.
|提供条件||1. 本件リソースは非営利機関にのみ提供し、学術研究にのみ利用することができる。 2. 謝辞の表明を必要とする。|
Schedule A（GFP-A, 英語版のみ）が追加で必要です。
|Catalog #||Resource name||Shipping form||Fee (non-profit org.)|
|RDB03347||AxCALNLEGFP (forward)||Virus, lysate of infected cell culture|
|Featured content||Cre-loxP and FLP-FRT System (English text)|
|Featured content||Control Vectors (English text)|
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This clone will be sequenced a portion and digested by restriction enzyme for examination.