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Ad5-dlX

E3-deleted adenovirus type 5

Catalog number RDB01747
Resource name Ad5-dlX
Alternative name E3-deleted adenovirus type 5
Clone info. Parent virus. E3-deleted adenovirus type5. A sourse of the DNA-TPC used in COS-TPC method.
Vector backbone Adenovirus
Size of vector backbone -
Growth remarks 5 percent FCS is fine.
Gene/insert name AdV_5 Adenovirus type 5
Depositor|Developer Saito, Izumu |
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External Database
AdV_5 Adenovirus type 5

            Reference sequence
              
             
            Remarks, protocol and/or map (gif) RDB01747.gif

            Distribution information

            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 for distribution In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature designated by the DEPOSITOR is requested (Saito, I., J. Virol., 54, 711-719(1985)).
            Ordering Please visit Information of Request for Distribution.[link] For for-profit-research purpose, please contact us. 
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            Material Transfer Agreement (MTA for use for not-for-profit academic purpose) [Word]
            提供案内 (日本国内) [open/close]

            提供条件 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 (Saito, I., J. Virol., 54, 711-719(1985))。
            提供依頼 手続きの詳細は、「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。
            提供依頼書 [Word]
            提供同意書 (MTA、非営利機関による非営利学術研究用)[Word]
            遺伝子組換え生物の受入れ確認書 [Word]
            備考 【追加提供依頼書】受入れ確認書(書式J)
            組換え体提供にかかる書式が必要です。

            Catalog # Resource name Availability Shipping form Fee (non-profit org.)
            RDB01747 Ad5-dlX Under QC test. Please contact us. Virus, lysate of infected cell culture

            check Please wait for results of QC test to be uploaded. This clone will be sequenced a portion for examination.

            How to cite this biological resource

            Materials & Methods section:

            The Ad5-dlX was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB01747).

            Reference section:

            Miyake, S., Makimura, M., Kanegae, Y., Harada, S., Sato, Y., Takamori, K., Tokuda, C., Saito, I., Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome. Proc. Natl. Acad. Sci. USA, 93, 1320-1324 (1996). PMID 8577762.
            Saito, I., Oya, Y., Yamamoto, K., Yuasa, T., Shimojo, H., Construction of nondefective adenovirus type 5 bearing a 2.8-kilobase hepatitis B virus DNA near the right end of its genome. J. Virol., 54, 711-719 (1985). PMID 3999192.

            Further references such as user reports and related articles (go to bottom)


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            References

            Original, user report and related articles

            original Miyake, S., Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome. Proc. Natl. Acad. Sci. USA, 93, 1320-1324 (1996). PMID 8577762.
            original Saito, I., Construction of nondefective adenovirus type 5 bearing a 2.8-kilobase hepatitis B virus DNA near the right end of its genome. J. Virol., 54, 711-719 (1985). PMID 3999192.
            user_report Ugai H., Accumulation of infectious mutants in stocks during the propagation of fiber-modified recombinant adenoviruses. Biochem. Biophys. Res. Commun. 337, 806-814 (2005). PMID 16214112.
            user_report Sato Y., Cell specificity and efficiency of the Semliki forest virus vector- and adenovirus vector-mediated gene expression in mouse cerebellum. J. Neurosci. Methods, 137, 111-121 (2004). PMID 15196833.

            2023.05.02

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