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Their dynamic and reversible nature enables rapid responses to intra- and extracellular signals that regulate cell death decisions by altering the membrane-binding capacity, stability, and interactions of substrate proteins [29]

Following this, the protein lysates were denatured in a metal bath at 95 C and subjected to SDS-polyacrylamide gel electrophoresis (SDS-PAGE) for separation

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Research data shows the dual-receptor approach generates a larger GH pulse amplitude than GHRH-only stimulation, making it a different research tool for studying secretagogue synergy rather than isolated GHRH signaling