Serum-free medium suitable to culturing ovary cells of Chinese hamster
A technology of Chinese hamster and ovary cells, applied in tissue culture, microorganisms, biochemical equipment and methods, etc., can solve problems such as high cost, lack of CHO cell culture, and influence on product separation and purification
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Embodiment 1
[0150] Orthogonal method to determine the best medium for CHO cell culture
[0151] On the basis of the initial medium, the concentrations of vitamin C, putrescine, and lipids were changed (see Table 1 below), and different mediums were prepared. The same number of the same CHO cells (2.0×10 5 Cells / mL) were inoculated in a 125ml square bottle filled with 10ml culture medium, at 37°C, CO 2 Culture in the incubator for about 8 days, and then measure the number of CHO cells.
[0152] Element
Content (mg / L)
5
5
2.5
Sodium Selenite
0.01
[0153] A
B
C
Vitamin C(mg / L)
Putrescine (mg / L)
lipid mixture * (v / v%)
1
5
2
0.1
2
10
5
0.2
3
30
10
0.5
[0154] arachidonic acid
2mg / L
cholesterol ...
Embodiment 2
[0158] Preparation of media and CHO cell culture
[0159] (a) Medium formula:
[0160] DMEM / F12 medium (purchased from Sigma company) and in it simultaneously add the following supplements:
[0161] L-alanine
[0162] AgNO 3
[0163] folic acid
[0164] insulin
[0165] In a 125mL cell culture square bottle, add 10mL of the medium prepared above, and then add CHO cells with glutamine synthetase expression system, the inoculation density is 2.0×10 5 Cells / mL, sampling and counting every 24 hours. at 37°C, CO 2 Cells were grown in an incubator. On the 8th day of cell culture, the viable cell density reached the highest, which was 1.1×10 6 cells / mL.
Embodiment 3
[0170] Wild-type CHO cell culture
[0171] The experiments of Example 2 and Comparative Example 1 were repeated, except that the wild-type CHO cells were used to replace the CHO cells with glutamine synthetase expression system, and aminosulfoxide-methionine was not added to the medium.
[0172] The highest viable cell density was 1.6 × 10 in serum- and serum-free media, respectively. 6 cells / mL and 1.8×10 6 cells / mL indicates that the serum-free medium of the present invention can completely replace the medium with serum for the cultivation of CHO cells.
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