| 產(chǎn)品名稱 | Primary Epidermal Melanocytes; Normal, Human, Neonatal (HEMn) | |||||||||||||||||||||||||||||||||||
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| 商品貨號 | B239180 | |||||||||||||||||||||||||||||||||||
| Organism | Homo sapiens, human | |||||||||||||||||||||||||||||||||||
| Tissue | Skin | |||||||||||||||||||||||||||||||||||
| Cell Type | Melanocyte | |||||||||||||||||||||||||||||||||||
| Morphology | Stellar, multipolar or dendritic apperance; needle-like | |||||||||||||||||||||||||||||||||||
| 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 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. |
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| Disease | Normal | |||||||||||||||||||||||||||||||||||
| Age | Neonatal | |||||||||||||||||||||||||||||||||||
| Gender | Male | |||||||||||||||||||||||||||||||||||
| Applications | Melanoma, response to UV radiation, psoriasis and other skin diseases, skin trauma (e.g., wound repair, scars, burns), cosmetic research (e.g., skin lightening compounds, skin protecting compounds) |
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| Product Format | frozen 1 mL | |||||||||||||||||||||||||||||||||||
| Storage Conditions | -130°C or below | |||||||||||||||||||||||||||||||||||
| Comments | ATCC® Normal Human Primary Epidermal Melanocytes (HEMn) from Neonatal Foreskin, when grown in Dermal Cell Basal Media supplemented with Melanocyte Growth Kit components, provide an ideal cell system to propagate melanocytes in low serum (less than 1.0% FBS) conditions in the absence of cholera toxin and phorbol 12-myristate 13-acetate (PMA). The cells are cryopreserved in the second passage to ensure the highest viability and plating efficiency. |
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| Complete Growth Medium |
Table 1. Melanocyte Growth Kit Components
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