HFF-1 Cells
545,10 CAD$*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
Renseignements généraux
| Description | HFF-1 is a human foreskin fibroblast cell line frequently used as a feeder layer for the culture of human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs). Derived from neonatal dermal tissue, HFF-1 cells provide essential extracellular matrix components and secrete key signaling molecules that promote hESC attachment and partially support their pluripotent state. These fibroblasts have been evaluated for their expression of several pluripotency-supporting growth factors, including TGFβ1, activin A, and fibroblast growth factor 2 (FGF-2), although their effectiveness as feeder cells can vary depending on the specific line and culture conditions. In comparative studies, human foreskin fibroblasts like HFF-1 secrete detectable levels of FGF-2 and activin A, though their secretion levels are generally lower than those observed in mouse embryonic fibroblasts. HFF-1 cells also express BMP-4 mRNA and protein, although secreted levels of BMP-4 dimers are extremely low and often undetectable in conditioned media, likely due to intracellular sequestration or inhibition by gremlin. Importantly, the secretion of growth factors by HFF-1 is modulated by mitotic inactivation (e.g., mitomycin C treatment) and media composition (e.g., KnockOut Serum Replacement vs. fetal bovine serum). The ability of HFF-1 cells to support undifferentiated hESC growth correlates with their secretion of activin A and TGFβ1, although supplementation with exogenous activin A can improve the maintenance of pluripotency markers such as SSEA3 when these cells are used as feeders. Overall, HFF-1 serves as a useful human-derived feeder cell model for stem cell culture systems aiming to reduce xeno-components. However, their capacity to maintain long-term undifferentiated hESC cultures is generally considered less robust than that of mouse-derived feeder cells unless combined with specific growth factor supplementation. Their human origin, however, makes them particularly attractive for clinical and translational stem cell applications where xeno-free conditions are essential. |
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| Organisme | Human |
| Tissu | Foreskin, skin |
| Synonymes | HFF1 |
Caractéristiques
| Âge | <1 month |
|---|---|
| Genre | Male |
| Morphologie | Fibroblast |
| Type de cellule | Fibroblast of foreskin |
| Propriétés de croissance | Adherent |
Données réglementaires
| Référence | HFF-1 (Cytion catalog number 305790) |
|---|---|
| Niveau de biosécurité | 1 |
| NCBI_Numéro d'identification fiscale | 9606 |
| Cellosaurus - Numéro d'enregistrement | CVCL_3285 |
Données biomoléculaires
| Profil mutationnel |
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Manipulation
| Milieu de culture | DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
|---|---|
| Suppléments | Supplement the medium with 15% FBS |
| Réactif de dissociation | Accutase |
| Renouvellement des fluides | 2 to 3 times per week |
| Milieu de congélation | As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. |
| Décongélation et culture des cellules |
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| Atmosphère d'incubation | 37°C, 5% CO2, humidified atmosphere. |
| Conditions d'expédition | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Conditions d'entreposage | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |
Contrôle de la qualité et analyse moléculaire
| Stérilité | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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Certificat d'analyse (CoA)
| Numéro de lot | Type de certificat | Date | Numéro de catalogue |
|---|---|---|---|
| 305790-221025 | Certificat d'analyse | 05. Dec. 2025 | 305790 |