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Cells were lysed in PBS/Triton X-100 (0.5%) for 60 min
Food and Drug Administrations decision last year that there was no longer a shortage of the medicines active ingredient, tirzepatide
0.008%, p 6.2 M (Figure S4d)
It is important to note that retatrutide has not received marketing authorisation from the Medicines and Healthcare products Regulatory Agency (MHRA) or the European Medicines Agency (EMA) , and no UK Summary of Product Characteristics (SmPC) or European Public Assessment Report (EPAR) exists for this medicine
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