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Skin Ethic Laboratories

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Skin Ethic Laboratories is a leader in tissue engineering and providing safety and efficacy tests for the Personal Care and Cosmetics industry. Their products include corneal epithelium, gingivalm epithelium, oral epithelium, vaginal epithelium, human epidermis, and pigmented epidermis. Testing applications include skin corrosion and irritation, ocular irritation, pigmentation, phototoxicity, and more.
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Episkin Skin Ethic Laboratories Episkin is an in vitro reconstructed human epidermis from normal human keratinocytes cultured on a collagen layer coated on an inert filter at the air-liquid interface. This model is histologically similar to the in vivo human epidermis.
HCE / Corneal Epithelium Skin Ethic Laboratories HCE / Corneal Epithelium is 0,5 cm² epithelium reconstituted by airlifted culture of transformed human keratinocytes for 5 days in chemically defined medium on inert polycarbonate filters.
HGE / Gingivalm Epithelium Skin Ethic Laboratories HGE / Gingivalm Epithelium is 0.5 cm² epithelium reconstituted by airlifted culture of transformed human keratinocytes for 5 days in chemically defined medium on inert polycarbonate filters.
HOE / Oral Epithelium Skin Ethic Laboratories HOE / Oral Epithelium is 0.5 cm² epithelium reconstituted by airlifted culture of transformed human keratinocytes for 5 days in chemically defined medium on inert polycarbonate filters.
HVE / Vaginal Epithelium Skin Ethic Laboratories HVE / Vaginal Epithelium is 0.5 cm² epithelium reconstituted by airlifted culture of transformed human keratinocytes for 5 days in chemically defined medium on inert polycarbonate filters.
RHE / Human Epidermis Skin Ethic Laboratories RHE / Human Epidermis is a 0.5 cm² reconstructed epidermis of normal human keratinocytes. Cells are grown on inert polycarbonate filter on chemically defined medium, airlifted for 17 days.
RHPE / Pigmented Epidermis Skin Ethic Laboratories RHPE / Pigmented Epidermis is 0.5 cm² epidermis reconstituted by air-lifted co-culture of normal human keratinocytes and melanocytes for 10 days on chemically defined medium on inert polycarbonate filters (seeding density K/M 10:1).