Editing Trypan Blue Staining (section)

==== Protocol ====

1. centrifuge an aliquot of cell suspension being tested for viability 5 min at 100 × g (1 ~2 min at 1000 rpm) and discard supernatant. The size of the aliquot depends on the approximate number of cells present. the aliquot should contain a convenient number of cells to count in a hemacytometer when suspended in 1 ml PBS and then diluted again by mixing with 0.4% trypan blue (e.g., 5 ×10^5 cells/ml). 

2. Resuspend the cell pellet in 1 ml pbs or serum-free complete medium. Serum proteins stain with trypan blue and can produce misleading results. determinations must be made in serum-free solution. 

3. mix 1 part of 0.4% trypan blue and 1 part cell suspension (dilution of cells). allow mixture to incubate 3 min at room temperature. 

Cells should be counted within 3 to 5 min of mixing with trypan blue, as longer incubation periods will lead to cell death and reduced viability counts. 

Mixing can be performed in a well of a microtiter plate or a small plastic tube using 10 to20 µl each of cell suspension and trypan blue. 

4. apply a drop of the trypan blue/cell mixture to a hemacytometer. place the hemacytometer on the stage of a binocular microscope and focus on the cells. 

5. count the unstained (viable) and stained (nonviable) cells separately in the hemacytometer. To obtain the total number of viable cells per ml of aliquot, multiply the total number of viable cells by 2 (the dilution factor for trypan blue). To obtain the total number of cells per ml of aliquot, add up the total number of viable and nonviable cellsand multiply by 2.<br> 

[[Category:Protocols]]