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CMT is a genetic disorder that occurs due to a gene mutation

Intended use: research use only

The REDEFINE 2 trial in patients with type 2 diabetes showed CagriSema achieved HbA1c levels of 6.5% or below in 73.5% of participants

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RPTEC were maintained in Renal Epithelial Cell Basal Medium (REBM, ATCC) supplemented with 0.5% FBS, 10 nM triiodothyronine, 10 ng ml 1 rh EGF, 100 ng ml 1 hydrocortisone hemisuccinate, 5 g ml 1 rh insulin, 1 M epinephrine, 5 g ml 1 transferrin and 2.4 mM L-alanyl-L-glutamine