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Primary Epidermal Melanocytes; Normal, Human, Neonatal (HEMn)
Primary Epidermal Melanocytes; Normal, Human, Neonatal (HEMn)
規(guī)格:
貨期:
編號(hào):B239180
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


              產(chǎn)品名稱 Primary Epidermal Melanocytes; Normal, Human, Neonatal (HEMn)
              商品貨號(hào) 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.

              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)
              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.
              Complete Growth Medium
              1. Obtain one Melanocyte Growth Kit from the freezer; make sure that the caps of all components are tight.
              2. Thaw the components of the growth kit just prior to adding them to the basal medium. It is necessary to warm the L-glutamine component in a 37°C water bath and shake to dissolve any precipitates prior to adding to the basal medium.
              3. Obtain one bottle of Dermal Cell Basal Medium (485 mL) 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.
              6.  Table 1. Melanocyte Growth Kit Components 

                Component

                Subculturing

                Volume

                Volume

                Final Concentration

                Cells per Vial

                rh Insulin

                Sterility Tests

                0.5 mL

                Viral Testing

                5 µg/ml

                Viability

                Ascorbic Acid

                Population Doubling Capacity

                0.5 mL

                C of A

                50 µg/ml

                梅經(jīng)理 17280875617 1438578920
                胡經(jīng)理 13345964880 2438244627
                周經(jīng)理 17757487661 1296385441
                于經(jīng)理 18067160830 2088210172
                沈經(jīng)理 19548299266 2662369050
                李經(jīng)理 13626845108 972239479
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