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            上海哈靈生物科技有限公司>技術(shù)文章>3T3-L1 小鼠胚胎成纖維細(xì)胞

            技術(shù)文章

            3T3-L1 小鼠胚胎成纖維細(xì)胞

            閱讀:956          發(fā)布時(shí)間:2017-1-17

            3T3-L1   小鼠胚胎成纖維細(xì)胞

            General Information:

            Organism:

            Mus musculus, mouse

            Tissue:

            embryo

            Culture Properties:

            adherent

            Morphology:

            fibroblast

             

            Culture Method:

            Complete Growth Medium:

            DMEM (Gibco 12800-017)+10% CS+ Penicillin/Streptomycin

            Subculturing:

            Volumes are given for a 25cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes. Never allow culture to become compley confluent.

            • Remove and discard culture medium.
            • Briefly rinse the cell layer with 0.25%(w/v) Trypsin- EDTA solution to remove all traces of serum that contains trypsin inhibitor.
            • Add 1.0 to 2.0mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed. Discard Trypsin-EDTA solution.
            • Add 6.0 to 8.0mL of complete growth medium and aspirate cells by gently pipetting.
            • Add appropriate aliquots of the cell suspension to new culture vessels.
            • Incubate cultures at 37°C, 5% CO2.

            Subc*tion Ratio:

            The recommended inoculum is 2~3×103cells/cm2. Subculture before cultures become 70 to 80% confluent or when cells reach 5 ~ 6×104 cells/cm2.

            Cryopreservation:

            Freeze medium: Complete growth medium supplemented with 10% (v/v) DMSO

            Storage temperature: liquid nitrogen vapor phase

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