1 [These primary cells are not known to harbor an agent recognized to cause disease in healthy adult humans. Handle as a potentially biohazardous material under at least Biosafety Level 1 containment. Cells derived from primate lymphoid tissue may fall under the regulations of 29 CFR 1910.1030 Bloodborne Pathogens.
ATCC recommends that appropriate safety procedures be used when handling all primary cells and cell lines, especially those derived from human or other primate material. Detailed discussions of laboratory safety procedures are provided in Laboratory Safety: Principles and Practice, 2nd ed. (ASM Press, Washington, DC) (Fleming et al., 1995) and Caputo, J.L. Biosafety procedures in cell culture. (1988) J. Tissue Culture Methods 11:223.
Appropriate safety procedures should always be used with this material. Laboratory safety is discussed in the following publication: Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS Publication No. (CDC) 93-8395. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online at http://www.cdc.gov/biosafety/publications/bmbl5/index.htm.]
Human Material Precaution
All tissues used for isolation are obtained under informed consent and conform to HIPAA standards to protect the privacy of the donor’s personal health information. It is best to use caution when handling any human cells. We recommend that all human cells be accorded the same level of biosafety consideration as cells known to carry HIV. With infectious virus assays or viral antigen assays, even a negative test result may leave open the possible existence of a latent viral genome.
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
Lot-specific
Gender
Lot-specific
Ethnicity
Lot-specific
Applications
An ideal culture model for the study or development of a potential diagnostic method for the early detection of bladder cancer cells, reconstruction studies, and advancement of cancer research.
Product Format
frozen 1.0 mL
Storage Conditions
-130oC or below
Comments
HBFC are cryopreserved at P2 and marketed as secondary cells (cells have been isolated, plated, and expanded in culture vessels twice prior to cryopreservation) to ensure the highest viability and proliferation efficiency.
These cells, when transiently transfected using TransfeX Transfection Reagent (ATCC® ACS-4005™), express high levels of GFP.
Complete Growth Medium
Obtain one vial of Primary Normal Bladder Fibroblast Cells (ATCC PCS-420-013) from the freezer? make sure that the caps of all components are tight.
Thaw the components of the growth kit (ATCC PCS-201-041) just prior to adding them to the basal medium (ATCC PCS-201-030).
Obtain one bottle of Fibroblast Basal Medium (485 mL; PCS-201-030) from cold storage.
Decontaminate the external surfaces of all growth kit component vials and the basal medium bottle by spraying them with 70% ethanol.
Using aseptic technique and working in a laminar flow hood or biosafety cabinet, transfer the
indicated volume of each growth kit component, as indicated in Table 1, to the bottle of basal medium
using a separate sterile pipette for each transfer.
Table 1. If using the Fibroblast Growth Kit-Low Serum, add the indicated volume for each of the following components
