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Primary Uterine Fibroblast Cells; Normal, Human (HUF) (ATCC® PCS-460-010)

Organism: Homo sapiens, human  /  Tissue: Uterus  /  Cell Type: Fibroblast

Permits and Restrictions

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Organism Homo sapiens, human
Tissue Uterus
Cell Type Fibroblast
Morphology Spindleshaped; cells are bipolar and refractile.
Growth Properties Adherent
Biosafety Level 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] 

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 Adult
Gender Female
Applications Applications for use might include research related to female reproductive biology; drug testing; and oncology.
Product Format frozen 1 mL
Storage Conditions -130°C or below

The cells (HUFs) are cryopreserved in the second passage to ensure the highest viability and plating efficiency. 

Fibroblast Basal Medium (ATCC PCS-201-030), when supplemented with Fibroblast Growth Kit-Low Serum (ATCC PCS-201-041), provides an ideal system to propagate uterine fibroblasts.

Characterization: TE-7 (+), Pan-Cytokeratin (-)

Complete Growth Medium
  1. Obtain one vial of Primary Uterine Fibroblasts; Normal, Human (ATCC PCS-460-010) from the freezer; make sure that the caps of all components are tight.
  2. Thaw the components of the growth kit (ATCC PCS-201-041) just prior to adding them to the basal medium (ATCC PCS-201-030).
  3. Obtain one bottle of Fibroblast Basal Medium-Low Serum (485 mL; PCS-201-041) from cold storage.
  4. Decontaminate the external surfaces of all growth kit component vials and the basal medium bottle by spraying them with 70% ethanol.
  5. 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. Fibroblast Growth Kit-Low Serum Components



    Final Concentration

    rh FGF b

    0.5 mL

    5 ng/mL


    18.75 mL

    7.5 mM

    Ascorbic acid

    0.5 mL

    50 µg/mL

    Hydrocortisone Hemisuccinate

    0.5 mL

    1 µg/mL

    rh Insulin

    0.5 mL

    5 µg/mL

    Fetal Bovine Serum

    10.0 mL




Antimicrobials and phenol red are not required for proliferation but may be added if desired. The recommended volume of either of the optional components to be added to the complete growth media is summarized in Table 2.

Table 2. Addition of Antimicrobials/Antimycotics and Phenol Red (Optional)



Final Concentration

Penicillin-Streptomycin-Amphotericin B Solution

0.5 mL

Penicillin: 10 Units/mL

Streptomycin: 10 µg/mL

Amphotericin B: 25 µg/mL

Phenol Red

0.5 mL

33 µM

  1. Tightly cap the bottle of complete growth medium and swirl the contents gently to assure a homogeneous solution. Do not shake forcefully to avoid foaming. Label and date the bottle.
  2. Complete growth media should be stored in the dark at 2°C to 8°C (do not freeze). When stored under these conditions, complete growth media is stable for 30 days.
  1. Passage normal uterine fibroblast cells when culture has reached approximately 80% confluence. 
  2. Warm both the Trypsin-EDTA for Primary Cells (ATCC PCS-999-003) and the Trypsin Neutralizing Solution (ATCC PCS-999-004) to room temperature prior to dissociation. Warm complete growth medium to 37°C prior to use with the cells. 
  3. For each flask, carefully aspirate the spent media without disturbing the monolayer. 
  4. Rinse the cell layer two times with 3 to 5 mL D-PBS (ATCC 30-2200) to remove residual traces of serum. 
  5. Add pre-warmed trypsin-EDTA solution (1 to 2 mL for every 25 cm2) to each flask. 
  6. Gently rock each flask to ensure complete coverage of the trypsin-EDTA solution over the cells, and then aspirate the excess fluid off of the monolayer. 
  7. Observe the cells under the microscope. When the cells pull away from each other and round up (typically within 3 to 5 minutes), remove the flask from the microscope and gently tap it from several sides to promote detachment of the cells from the flask surface. 
  8. When the majority of cells appear to have detached, quickly add an equal volume of Trypsin Neutralizing Solution (ATCC PCS-999-004) to each flask. Gently pipette or swirl the culture to ensure all of the trypsin-EDTA solution has been neutralized. 
  9. Transfer the dissociated cells to a sterile centrifuge tube and set aside while processing any remaining cells in the flask. 
  10. Add 3 to 5 mL D-PBS (ATCC 30-2200) to the flask to collect any additional cells that might have been left behind. 
  11. Transfer the cell/D-PBS suspension to the centrifuge tube containing the trypsin-EDTA-dissociated cells. 
  12. Repeat steps 10 and 11 as needed until all cells have been collected from the flask. 
  13. Centrifuge the cells at 150 x g for 3 to 5 minutes. 
  14. Aspirate the neutralized dissociation solution from the cell pellet and resuspend the cells in 2 to 8 mL fresh, pre-warmed, complete growth medium. 
  15. Count the cells and seed new flasks at a density of 2,500 to 5,000 cells per cm2
  16. Place newly seeded flasks in a 37°C, 5% CO2, incubator for at least 24 to 48 hours before processing the cells further. Refer to Maintenance for guidelines on feeding.
Volume 1 mL
Sterility Tests Bacteria and Yeast: Negative
Mycoplasma: Negative
Viral Testing Hepatitis B: Negative
Hepatitis C: Negative
HIV: Negative
Viability ≥ 70% when thawed from cryopreservation
Population Doubling Capacity ≥ 10 in complete growth medium
C of A
Certificate of Analysis
Certificate of Analysis
Notice: Necessary PermitsPermits

These permits may be required for shipping this product:

  • Customers located in the state of Hawaii will need to contact the Hawaii Department of Agriculture to determine if an Import Permit is required. A copy of the permit or documentation that a permit is not required must be sent to ATCC in advance of shipment.
Basic Documentation

Sun M, et al. Scissor-Like Chiral Metamolecules for Probing Intracellular Telomerase Activity. WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2016. DOI: 10.1002/adfm.201601942

Li S, et al. Hybrid Nanoparticle Pyramids for Intracellular Dual Micrornas Biosensing and Bioimaging. Adv Mater 19(29), 2017. PubMed: 28221715

Ma W, et al. A Chiral-Nanoassemblies-Enabled Strategy for Simultaneously Profiling Surface Glycoprotein and MicroRNA in Living Cells. Adv Mater 29(42), 2017. PubMed: 28980743

Zhao X, et al. Gold-Quantum Dot Core-Satellite Assemblies for Lighting up Microrna in Vitro and in Vivo. Small 34(12):4662-8, 2016. PubMed: 26849492

Chen B, et al. Energy transfer-based biodetection using optical nanomaterials. J Mater Chem B 6:2924-2944, 2018. DOI: 10.1039/C8TB00614H