Swine testicular cell strain ST-S suitable for suspension culture as well as acquisition method and application of swine testicular cell strain ST-S
A technology of suspension culture and porcine testis, applied in the field of cell engineering, can solve the problems of limiting the application scale and production efficiency of ST cells
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Embodiment 1
[0078] Embodiment 1, obtaining the ST-S cell that can be cultured in suspension
[0079] In this example, by developing a personalized culture medium and optimizing the domestication approach, a pig testis cell strain that can be cultured in complete suspension under low serum conditions was finally obtained, named ST-S. Specifically, the cell strain ST-S of the present invention The method of obtaining includes the following steps:
[0080] 1. Domestication of adherent ST cells in plastic culture flasks
[0081] Usually, the subculture ratio of ST cells adherently cultured in a square culture flask is 1:3, that is, after the cells grow into a monolayer in a T75 plastic culture square flask, trypsin digestion solution (it is better to cover the cell surface, About 5 mL) of the cell suspension obtained after digestion can be evenly inoculated in three T75 plastic culture square flasks (Welter, M.W., Welter, C.J., Chambers, D.M., and Svensson, L. (1991) Adaptation and serial pa...
Embodiment 2
[0155] Embodiment 2, suspension culture ST-S cell in 5L bioreactor
[0156] The ST-S cell strain of the present invention still has the characteristics of suspension culture after cryopreservation. After the cryopreserved ST-S cell line is revived, it does not need to be acclimatized, and can be directly enlarged for suspension culture. This example provides a semi-fed-batch suspension culture method in a 5L bioreactor after recovery of the ST-S cell line.
[0157] Suspension culture of ST-S cells in a 5L reactor includes the following steps:
[0158]1) Resuscitating the frozen ST-S cell line, the method is: take out a frozen ST-S cell line (obtained in Example 1) from liquid nitrogen, thaw it quickly in a 37°C water bath, add the pre-prepared ( Put the medium in a 10mL centrifuge tube containing 5mL ST-LSM-s medium (preheated at 37°C for 10 minutes), centrifuge at 1000rpm for 5 minutes, pour off the supernatant, resuspend the cells with ST-LSM-s medium, and transfer the cel...
Embodiment 3
[0164] Embodiment 3, detect the sensitivity of ST-S cell to classical swine fever virus
[0165] This example is used to understand the susceptibility of suspension cultured ST-S cells to classical swine fever virus (CSFV), and compare it with adherent cultured ST cells.
[0166] 1. Cells infected by CSFV virus
[0167] 1. Infect adherent ST cells with CSFV virus: cryopreserved adherent ST cells were inoculated into T75 glass culture flasks after thawing and cultured in T25 glass culture flasks, at an inoculation density of 3×10 4 cells / cm 2 , the culture medium is ST-LSM-s medium containing 3% calf serum, and the culture volume is 20 mL. When the cells were cultured to a confluence of 70-80%, they were inoculated with CSFV spleen virus (purchased from Jinyu Baoling Biopharmaceutical Co., Ltd.) at 0.4% (M / V).
[0168] 2, CSFV virus infection suspension ST cells (ST-S): frozen ST-S cells (obtained by suspension culture according to the method of Example 2) were revived and i...
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