Culture Type: | Cell line |
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Collection: | ECACC General Collection |
Catalogue No.: | 15042902 |
Cell Line Name: | CHO-K1.Cl7 |
Organisation deposited by: | Cambridge Enterprise |
Other Collection No.: | N/A |
Unique to ECACC: | Yes |
Citation Guidance: | If use of this culture results in a scientific publication, it should be cited in the publication as: CHO-K1.CI7 (ECACC 15042902) |
Keywords: | CHO-K1, FcγRIIIa , Fc gamma receptor 3A, 158F, allotype, human IgG , IgG binding |
Cell Line Description: | Clone of CHO-K1 cells expressing human FcγRIIIa of the 158F allotype anchored to glycosyl phosphatidylinositol |
Species: | Hamster |
Tissue of Origin: | Ovary |
CellType: | Epithelial |
Morphology: | Polygonal |
Growth Mode: | Adherent |
DNA Profile: | n/a |
Karyotype: | N/A |
GMO Status: | Genetically Modified Organism Class 1 (GMO1) |
Genetic Modification: | Stably transfected with a pcDNA3.1/Hygro(+) based vector with a human FcγRIIIa 158F cDNA insert that had been modified to enable expression as a GPI linked receptor |
Hazard Group (ACDP): | 2 |
Subculture Routine: | Split sub-confluent cultures (70-80%) 1:3 to 1:6. Seeding at 2-5 x 10,000 cells/cm² using 0.05% trypsin/EDTA; culture conditions 5% CO2/95%air; 37°C |
Culture Medium: | EMEM (EBSS) + 2mM Glutamine + 1% Non- Essential Amino Acids (NEAA) + 10% Foetal Bovine Serum (FBS) with 600ug/ml hygromycin B |
Depositor: | Dr Kathryn L Armour |
Originator: | Yes |
Country: | UK |
References: | Armour KL, Smith CS, Clark MR. Expression of human Fc gamma RIIIa as a GPI-linked molecule on CHO cells to enable measurement of human IgG binding. J Immunol Methods. 2010 Mar 31;354 (1-2):20-33. doi: 10.1016/j.jim.2010.01.011. Epub 2010 Feb 4. PMID:20138184 [PubMed - indexed for MEDLINE |
Additional Bibliography: | Armour KL, Smith CS, Turner CP, Kirton CM, Wilkes AM, Hadley AG, Ghevaert C, Williamson LM, Clark MR. Low-affinity FcγR interactions can decide the fate of novel human IgG-sensitised red blood cells and platelets. Eur J Immunol. 2014Mar; 44 (3):905-14. doi: 10.1002/eji.201343825. Epub 2014 Feb 16. PubMed Armour KL, Smith CS, Ip NC, Ellison CJ, Kirton CM, Wilkes AM, Williamson LM, Clark MR. Clearance of human IgG1-sensitised red blood cells in vivo in humans relates to the in vitro properties of antibodies from alternative cell lines. PLoS One. 2014 Oct 10;9(10):e109463. doi: 10.1371/journal.pone.0109463. eCollection 2014. PubMed PMID: 25302805; PubMed Central PMCID: PMC4193810. PMID:24285214; PubMed Central PMCID: PMC4209800. Harrison A, Liu Z, Makweche S, Maskell K, Qi H, Hale G. Methods to measure the binding of therapeutic monoclonal antibodies to the human Fc receptor Fc?RIII (CD16) using real time kinetic analysis and flow cytometry. J Pharm Biomed Anal. (2012); 63:23-8. PMID:22366323 Rohatgi S, Gohil S, Kuniholm MH, Schultz H, Dufaud C, Armour KL, Badri S, Mailliard RB, Pirofski LA. Fc gamma receptor 3A polymorphism and risk for HIV-associated cryptococcal disease. MBio. 2013; 4(5):e00573-13. PMID: 23982074 PMCID: PMC3760251 |
Patents: | None |
Release Conditions: | Yes - commercial organisations are required to complete the 'Cell Line Release Authorisation for Research Use in Commercial Organisations' release conditions form |
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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