High-migration-activity UCMSCs, culture method and application of key active components
A culture method and active technology, applied in the field of cells, to achieve the effect of promoting migration
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Embodiment 1
[0021] 1. Test materials
[0022] DMEM / F12 medium and fetal bovine serum were purchased from Gibco. Double antibodies were purchased from Nanjing Senbega Biotechnology Co., Ltd. The PBS buffer was prepared according to the recipe and stored at 4°C, and used up within 24 hours. Type IV collagenase and trypsin were purchased from Shanghai Maokang Biotechnology Co., Ltd. and used according to the instructions. S-allyl-L-cysteine was purchased from source leaf organisms, HPLC≥98%. Cell culture dishes, multi-well plates and Transwell chambers were purchased from Corning. The primary and secondary antibodies of SOX2, NANOG, OCT4 and β-actin were purchased from Beyond Biotech.
[0023] 2. Test method
[0024] 1. Preparation of UCMSCs
[0025] Prepare UCMSCs according to conventional methods, specifically: take about 12 cm of umbilical cord of normal full-term caesarean section neonates (the umbilical cord is stored in PBS buffer containing 1% double antibody at 4°C after coll...
Embodiment 2
[0049] A medium for improving the migration activity of UCMSCs, using DMEM / F12 as a base medium, and adding effective concentration of S-allyl-L-cysteine to the base medium.
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