Technological process of producing recombinant human histiotype plasminogen activator TNK mutant
A technology of plasminogen and process method, which is applied in the field of production of recombinant human tissue plasminogen activator mutants, can solve the problem that the production method of recombinant human tissue plasminogen activator mutants has no literature reports, protease Inhibition of activity and other issues, to achieve the effect of low cost, simple equipment and simple process conditions
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[0022] 1 Construction of engineered cell lines
[0023] 1.1 Materials, methods and results
[0024] 11.1 Materials
[0025] 1.1.1.1 Strains
[0026] E. coli XL1-Blue (genotype hsdR17, supE44, recA1, endA1, gyrA46, thi, relA1, lac / F'[proAB+, lac Iq, lacZDM15::Tn10(tet r)]).
[0027] 1.1.1.2 Cell lines
[0028] CHO (dhfr - ), dihydrofolate reductase-deficient Chinese hamster ovary cells.
[0029] 1.1.1.3 Tool enzymes
[0030] Various restriction enzymes, T4 DNA ligase, alkaline phosphatase, and Taq DNA polymerase were purchased from Promega. Vent DNA polymerase was purchased from Biolab Company. DNA molecular weight standards DL2000 (2000, 1000, 750, 500, 250, 100bp) and lamda-DNA / EcoRI (23130, 9416, 6557, 4361, 2322, 2027, 564, 125bp) were purchased from Treasure Bioengineering Dalian Co., Ltd.
[0031] 1.1.1.4 Main reagents
[0032] 1.1.1.4.1 3mM HT (hypoxanthine + thymine) concentrate
[0033] Hypoxanthine (purchased from Sigma Company) 40.83 mg, thymine (Sigma Comp...
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