The process for recombinant Human CBX5 protein synthesis in e.coli cells includes recombining the DNA fragment that encodes the Human CBX5 protein (1-191aa) into expression vector, transforming the recombinant vector into e.coli cells, screening positive cells, cultivating and inducing cells, conducting cell lysis, and performing expression analysis. The resulting recombinant Human CBX5 protein is purified from the cell lysate using affinity purification, with its purity exceeding 85% as determined by SDS-PAGE.
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