Shuttle vector to generate rAd harboring human GFRA1 (reverse)
|Resource name||pAxCALNLhGFRA1 (reverse)|
|Clone info.||Shuttle vector to generate rAd harboring GFRA1 Sugano full-length cDNA clone. Cre-recombinase is required to remove stuffer sequence.
Cre-recombinase is required to remove LNL stuffer sequence. Use COS-TPC method for the production of adenovirus.
|Vector backbone||Cosmid, use packaging extracts for transformation|
|Gene/insert name||Human GFRA1 cDNA|
|Depositor||DNA Bank, ||
|Other clones in our bank||human GFRA1 (NCBI Gene 2674) ||
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||In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature (Gene 200: 149-156, 1997) and acknowledgement to the DNA Bank are requested.|
|Ordering||Please visit Information of Request for Distribution. |
Order form [Credit Card Payment] [Bank Transfer or Check Payment]
Material Transfer Agreement (MTA) [Word]
|Remarks||Remember that you will be working with samples containing infectious virus. |
|提供条件||研究発表に際し、理研DNA Bankヘの謝辞ならびに次の論文の引用を必要とする (Gene 200: 149-156, 1997)。|
|Catalog #||Resource name||Availability||Shipping form||Fee (non-profit org.)|
|RDB05147||pAxCALNLhGFRA1 (reverse)||Under QC test. Please contact us.||DNA solution|
Further references such as user reports and related articles (go to bottom)
This clone will be sequenced a portion and digested by restriction enzyme for examination.
Original, user report and related articles