For research use only
| Cat No. | ABC-TC3184 |
| Product Type | Mouse Primary Cells |
| Cell Type | Epithelial |
| Species | C57BL/6 Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Dermal |
| Disease | Normal |
| Storage | Liquid Nitrogen |
C57BL/6 Mouse Primary Dermal Epithelial Cells from AcceGen are isolated from tissue of pathogen-free laboratory mice.
C57BL/6 Mouse Dermal Epithelial Cells are primary cells isolated from mouse dermal tissue. These cells primarily reside within the stratified squamous epidermis and hair follicle epithelial compartments. Following primary culture, these cells are cryopreserved. These cells are capable of self-renewal and maintain skin barrier integrity. Studies confirm their implication in psoriasis, chronic non-healing diabetic wounds, and cutaneous squamous cell carcinoma (UV-induced Trp53 mutations). Phenotypic characterization confirms expression of epithelial markers E-cadherin and ZO-1, validating their epithelial identity and junctional integrity. Repeated freezing and thawing should be avoided during culture. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | C57BL/6 Mouse Dermal Epithelial Cells, Mouse Dermal Epithelial Cells, Dermal Epithelial Cells, Epithelial Cells, EpiCs, C57BL/6 Dermal EpiCs |
| Species | C57BL/6 Mouse |
| Cat.No | ABC-TC3184 |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Epithelial |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Dermal |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Mouse Primary Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
C57BL/6 Mouse Dermal Epithelial Cells can be used as an in vitro model to study the pathogenesis of chronic wound healing disorders in disease conditions such as diabetic foot ulcers and psoriasis. For example, by investigating molecular pathways like TGF-β1/Smad3-mediated epithelial-mesenchymal transition impairment or IL-23/STAT3-driven keratinocyte hyperproliferation, these cells serve as a critical model to elucidate mechanisms of re-epithelialization failure, dysregulated immune responses, and epidermal barrier dysfunction.
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).