| Permits and Restrictions |
View Permits |
|---|---|
| Organism | Cercopithecus aethiops |
| Tissue | kidney |
| Product Format | frozen |
| Morphology | epithelial |
| Culture Properties | adherent |
| Biosafety Level |
1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Disease | Normal |
| Age | adult |
| Storage Conditions | liquid nitrogen vapor temperature |
| Derivation | VERO 76 was derived in 1968 by K.M. Johnson and brought to Centers for Disease Control (CDC), Atlanta, GA. It is a derivative of the original VERO. |
|---|---|
| Comments | When infected with hemorrhagic fever viruses [Machupo (Bolivian), Junin (Argentinian), Lassa (African)], Marburg or Ebola viruses, these cells exhibited cytopathic effects. Plaques are also produced. VERO 76 has a lower saturation density than the original VERO (ATCC CCL-81). |
| Complete Growth Medium | The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%. |
|---|---|
| Subculturing | Remove medium, and rinse with 0.25% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37°C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Subcultivation Ratio: A subcultivation ratio of 1:8 is recommended Medium Renewal: 2 to 3 times per week |
| Cryopreservation | Freeze medium: Complete growth medium 95%; DMSO, 5% Storage temperature: liquid nitrogen vapor temperature |
| Culture Conditions | Temperature: 37°C |
| Name of Depositor | EM Earley |
|---|---|
| Year of Origin | 1968 |
| References |
Earley EM, Johnson KMThe lineage of Vero, Vero 76 and its clone C1008 in the United StatesIn: Earley EM, Johnson KMVero cells: origin, properties and biomedical applicationsTokyoChiba Univ.pp. 26-29, 1988 Policastro PF, et al. Improved plaque assays for Rickettsia prowazekii in Vero76 cells. J. Clin. Microbiol. 34: 1944-1948, 1996. PubMed: 8818887 Schramm N, et al. Vesicles containing Chlamydia trachomatis serovar L2 remain above pH 6 within HEC-1B cells. Infect. Immun. 64: 1208-1214, 1996. PubMed: 8606080 |