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snRNA-seq and analysis For isolation of nuclei from gWAT, fresh adipose tissue was minced in nucleus preparation buffer (10 mM HEPES, 1.5 mM MgCl 2 , 10 mM KCl, 250 mM sucrose, 0.001% NP-40) with 0.2 U l Roche Protector RNase inhibitor followed by dounce homogenization

Lyophilized (Dry Powder) Unopened Vials Unopened lyophilized vials should be stored away from direct light and heat

Photostability evaluation To test the photostability in buffer and cell culture media, PLGA nanoparticles encapsulating DDA-GSH-AuNCs in water (2 mg/mL) was mixed with water (control), PBS or DMEM that contains 10% FBS (final concentration of PLGA nanoparticles is 0.5 mg/mL and AuNCs 4 g/mL as gold)

Unlike traditional fat-loss peptides, SLU-PP-332 works on pathways that mimic the benefits of exercise at the cellular level, making it an exciting option for weight management and metabolic health