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Trypsin-EDTA for Primary Cells is a low-concentration formulation (0.05% Trypsin and 0.02% EDTA in phosphate buffered saline without calcium or magnesium) of porcine pancreatic trypsin and EDTA that is suitable for the dissociation of cell monolayers that are susceptible to "over-trypsinization." These adherent cells include primary cells (i.e., ATCC® Primary Cells Solutions™ cell types) as well as a variety of mammalian cell lines that are propagated in serum-free or low serum conditions. Please refer to the product sheet supplied with each primary cell for details as to use, or contact ATCC Technical Service.

This product does not contain phenol red.

1. Bring the DPBS, the Trypsin-EDTA for Primary Cells, and the Trypsin Neutralizing Solution to room temperature before use. Warm the complete growth medium to 37°C prior to use with the cells.
2. For each flask, carefully aspirate the spent media without disturbing the monolayer. If the cell culture medium contains serum, each flask should be rinsed with DPBS twice prior to adding the Trypsin-EDTA for Primary Cells.
3. Using 1 to 2 mL for every 25 cm², add the appropriate volume of trypsin-EDTA solution to each flask (e.g., each T-25 flask would be dissociated with 1 to 2 mL trypsin-EDTA).
4. Gently rock each flask to ensure complete coverage of the trypsin-EDTA solution over the cells, and then aspirate the excess fluid off of the monolayer; do not aspirate to dryness.
5. Observe the cells under the microscope. When the cells pull away from each other and round up (typically within about 3 to 6 minutes), remove the flask from the microscope and gently tap the culture flask from several sides to promote detachment of the cells from the flask. Do not over-trypsinize as this will damage the cells.
   a. Some strongly adherent cell types, such as keratinocytes, may take much longer and may require trypsinization at 37°C.
   b. Some cell types may require more vigorous tapping.
6. When the majority of cells appear to have detached, quickly add an equal volume of the Trypsin Neutralizing Solution to each flask. Gently pipette or swirl the culture to ensure all of the trypsin-EDTA solution has been neutralized.
7. Transfer the dissociated cells to a sterile centrifuge tube and set aside while processing any remaining cells in the culture flask
8. Add 3 to 5 mL DPBS to the tissue culture flask to collect any additional cells that might have been left behind.
9. Transfer the cell / DPBS suspension to the centrifuge tube containing the trypsin-EDTA-dissociated cells.
10. Repeat steps 8 and 9 as needed until all cells have been collected from all flasks.
11. Centrifuge the cells at 150 x g for 3 to 5 minutes.
    a. Do not over centrifuge cells as this may cause cell damage.
    b. After centrifugation, the cells should form a clean loose pellet.
12. Aspirate neutralized dissociation solution and resuspend the cell pellet in 2 to 8 mL fresh, pre-warmed, complete growth medium.
13. Count the cells and seed new culture flasks at the recommended density.
14. Place newly seeded flasks in a 37°C, 5% CO2 incubator and incubate for at least 24 to 48 hours before processing the cells further.