|Supplied by:||European Collection of Authenticated Cell Cultures (ECACC)|
|Culture Type:||Cell line|
|Collection:||ECACC General Collection|
|Cell Line Name:||T26J-1/09 (CHO-Beta-2 (ADRB2))|
|Citation Guidance:||If use of this culture results in a scientific publication, it should be cited in the publication as: T26J-1/09 (CHO-Beta-2 (ADRB2)) (ECACC 10031601)|
|Keywords:||Human Adrenergic Receptor beta-2, ADRB2, G Protein Coupled Receptor, GPCR, Transfected, InSCREENeX SCREENflexTM, CHO-K1 Host.|
|Cell Line Description:||T26J-1/09 is clonally-derived from a CHO-K1 cell line which has been transfected with a human adrenergic receptor beta-2 G Protein Coupled Receptor (GPCR) cassette to allow expression of the human beta-2 GPCR. T26J-1/09 is an example of a cell line transfected using InSCREENeX SCREENflexTM|
|Tissue of Origin:||Ovary|
|GMO Status:||Genetically Modified Organism Class 1 (GMO1)|
Unless specified otherwise, at the European Collection of Authenticated Cell Cultures (ECACC) we routinely handle all of our cell lines at containment level 2 in accordance with the ACDP guidelines. ACDP = Advisory Committee on Dangerous Pathogens (UK)
All cell cultures have the potential to carry as yet unidentified adventitious agents. It is the responsibility of the end user to ensure that their facilities comply with biosafety regulations for their own country.
ACDP Guidance: Biological agents: Managing the risks in laboratories and healthcare premises.
Hyperlinks to MSDS documents:
Frozen cell cultures Material Safety Data Sheet
Growing cell cultures Material Safety Data Sheet
Nucleic acids derived from cell cultures Material Safety Data Sheet
|Subculture Routine:||Split sub-confluent cultures (70-80%) 1:4 to 1:10 i.e. seeding at 2 x 104 cells/cm² using 0.25% trypsin or trypsin/EDTA; 5% CO2; 37°C.|
|Culture Medium:||Ham's F12 + 2mM Glutamine + 10% Foetal Bovine Serum (FBS).|
|Depositor:||Dr Roland Schucht, InSCREENeX GmbH, Inhoffenstrasse 7, 38124 Braunschweig, Germany|
|References:||Schucht R, Coroadinha AS, Zanta-Boussif MA, Verhoeyen E, Carrondo MJ, Hauser H, Wirth D. (2006) A new generation of retroviral producer cells: predictable and stable virus production by Flp-mediated site-specific integration of retroviral vectors. Mol Ther. 14(2):285-92 PMID: 16697259.|
|Additional Bibliography:||Nehlsen K, Schucht R, da Gama-Norton L, Krömer W, Baer A, Cayli A, Hauser H, Wirth D. (2009) Recombinant protein expression by targeting pre-selected chromosomal loci. BMC Biotechnol. 9:100 PMID: 20003421. Schucht R, Wirth D, May T. (2010) Precise regulation of transgene expression level and control of cell physiology. Cell Biol Toxicol. 26(1):29-42 PMID: 19763851.|
|Patents:||None Specified By Depositor|
|Release Conditions:||Yes. All customers are required to complete a Material Transfer Agreement-SCREENflexTM Cell Lines. NOT TO BE TRANSFERRED TO OR USED IN THE UNITED STATES OF AMERICA.|
The Culture Collections represent deposits of cultures from world-wide sources. While every effort is made to ensure details distributed by Culture Collections are accurate, Culture Collections cannot be held responsible for any inaccuracies in the data supplied. References where quoted are mainly attributed to the establishment of the cell culture and not for any specific property of the cell line, therefore further references should be obtained regarding cell culture characteristics. Passage numbers where given act only as a guide and Culture Collections does not guarantee the passage number stated will be the passage number received by the customer.
Cultures supplied by Culture Collections are for research purposes only. Enquiries regarding the commercial use of a cell line are referred to the depositor of the cell line. Some cell lines have additional special release conditions such as the requirement for a material transfer agreement to be completed by the potential recipient prior to the supply of the cell line. Please view the Terms & Conditions of Supply for more information.
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