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- W2368909423 abstract "Objective: To obtain and purify rhcTnI. Methods: cDNA encoding cTnI was amplified from heart muscle cDNA library by PCR and then subcloned into prokarytic vector with a thrombin linker. MS2 cTnI fusion protein was expressed in E.coli . Results: Up to 30% of total bacterial proteins were rhcTnI as shown in SDS PAGE gel. The rhc TnI was purified to 95% homogeneity. Conclusion: rhc TnI can be expressed in E.coli in high quantity and purified to hear homogeneity." @default.
- W2368909423 created "2016-06-24" @default.
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- W2368909423 date "2000-01-01" @default.
- W2368909423 modified "2023-09-25" @default.
- W2368909423 title "The expression and purification of human cTnI overexpressed in E.coli" @default.
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