Cell line for stable expression of chicken interleukin 10 protein, as well as construction method and application thereof
A stable expression and cell line technology, which is applied in the field of preparation of recombinant chicken interleukin-10 protein, can solve the problems of low expression efficiency and unstable expression, and achieve the effect of wide application prospects
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Embodiment 1
[0034] Example 1 Construction of a cell line stably expressing chicken interleukin-10 protein
[0035] 1. Experimental method
[0036] 1.1 Isolation, culture and total RNA extraction of chicken peripheral blood lymphocytes
[0037] Collect 10 mL of sodium citrate anticoagulant blood from an adult SPF chicken through sterile wing vein, and separate peripheral blood lymphocytes with chicken lymphocyte separation medium according to the product instructions. Adjust the cell density to 1×10 with complete RPMI1640 medium containing 10% fetal bovine serum 6 / mL, added to 6-well cell plate culture, and added LPS with final concentrations of 10ug / mL and 20ug / mL and ConA with final concentrations of 10ug / mL, 25ug / mL and 30ug / mL as stimulators, At 37°C, 5% CO 2 The cells were cultured in an incubator, shaken every 4 h, and the cells were collected at different times. Total cellular RNA was extracted with Trizol Reagents total RNA extraction kit, and the specific method was carried o...
Embodiment 2
[0058] Example 2 Identification of cell lines stably expressing chicken interleukin-10 protein
[0059] 1. experimental method
[0060] 1.1 RT-PCR detection
[0061] Trizol Reagents extraction kit was used to extract the total RNA of CHO-chIL-10F and CHO-chIL-10M cells constructed in Example 1, and the specific method was carried out according to the instructions of the kit. The reverse transcription product cDNA was taken, and the chIL-10 gene was identified by PCR amplification. The reaction program was: 95°C for 5 minutes; 30 cycles of 94°C for 30s, 64°C for 30s, and 72°C for 40s; 72°C for 10 minutes.
[0062] 1.2 IFA detection
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