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METHOD FOR PERFORMING THE CYQUANT ASSAY USING A CELL-BASED STANDARD
CURVE
Prepare cells to be assayed for proliferation
Step 1. Detach adherent cells from the culture plate using a
trypsin or EDTA solution, and use culture medium to dilute the cell
suspension into a 96-well microplate, making the cell concentrations
(number of cells/well) shown in the template setup in Table 1. Include
a set of control wells without cells.
Table 1. Cell Concentration (Number Of Cells)
Prepared In A Microplate
Well
1
2
3
4
5
6
7
8
9
10
11
12
A
50,000
25,000
12,500
6,250
3,125
1,562
391
195
98
49
24
no cells
B
50,000
25,000
12,500
6,250
3,125
1,562
391
195
98
49
24
no cells
C
50,000
25,000
12,500
6,250
3,125
1,562
391
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