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Quantity limit per order for this item is 1. This item can be ordered twice a year. Orders over this limit will be sent to NIAID for approval before shipment.
ARP-1109 cells express human CD4 protein on the cell surface and can be infected by most isolates of human immunodeficiency virus (HIV). HeLa cells were infected with a retroviral vector expressing CD4 and Neor. Clones were selected for neomycin resistance and screened for the presence of surface CD4 via indirect immunofluorescence. Morphology is variable epithelial.
Foci of ARP-1109 infected with HIV-1 can be detected by indirect immunoperoxidase or immunofluorescence using anti-HIV-1 serum or monoclonal antibodies, or at a lower efficiency by syncytia formation. These cells are more sensitive than HT4-6C cells for titration of isolates from AIDS patients, giving endpoint titration values similar to PBLs. However, enhanced sensitivity in titration of laboratory-adapted HIV strains is not seen. Cells can be grown in the presence of G418. Clone 1022 cells contain no ecotropic or amphotropic murine retrovirus env genes.
Growth Characteristics: ARP-1109 is a rapidly growing cell line with a doubling time of about 38 hours. Cultures should be passaged by trypsinizing every 4 to 7 days at a ratio of 1:5 to 1:10. Cultures should be used to seed for HIV focal infectivity when cell density is subconfluent when density is < 3 × 106 in a 25 cm2 flask. For long-term passage, maintain cells in 1.0 mg per mL G418. During the rapid expansion of cells to attain the numbers necessary for assays, G418 may be omitted.
Growth Medium: RPMI 1640 medium supplemented with 10% fetal bovine serum and 1.0 mg per mL G418
ARP-1109 is negative for Mycoplasma, bacteria and fungi.
Each vial of ARP-1109 contains approximately 3.5 × 106 cells per mL in RPMI 1640 supplemented with 40% fetal bovine serum and 10% dimethyl sulfoxide (DMSO). Please refer to the appropriate data sheet for lot-specific information.
Chesebro, B. and K. Wehrly. “Development of a Sensitive Quantitative Focal Assay for Human Immunodeficiency Virus Infectivity.” J. Virol. 62 (1988): 3779-3788. PubMed: 3047430. Chesebro, B., et al. “Failure of Human Immunodeficiency Virus Entry and Infection in CD4-Positive Human Brain and Skin Cells.” J. Virol. 64 (1990):215-221. PubMed: 2293663.
Chesebro, B., et al. “CD4-Positive HeLa Cell Clone for Direct Quantitation of Infectious Human Immunodeficiency Virus from Blood Cells.” J. Infect. Dis. 163 (1991): 64-70. PubMed: 1984477.
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