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For cloning of the MCP transfer vector, the first 215 aa of the N-terminal MCP sequence were truncated and replaced by a glutathione-S-transferase (GST)-tag

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This crucial step removes impurities, improves stability, and protects the integrity of the formula

Full-Length: Comparison of fragment effects to full-length hGH actions Mechanism Dissection: Investigation of how C-terminal fragment exerts metabolic effects Receptor Identification: Research on potential alternative receptors or binding proteins This research area addresses fundamental questions about growth hormone biology and functional domain organization