Cryo-focused ion beam (cryo-FIB) milling is indispensable for preparing thin lamellae from thick biological samples for cryo-electron tomography (cryo-ET), especially at the tissue level. However, existing approaches remain technically demanding and susceptible to lamella instability. We present a detailed, optimized serial lift out cryo-FIB milling protocol specifically designed for multicellular tissue samples, emphasizing improved lamella stability, reproducibility, and reduced operator dependency. This method integrates six-sided attachment geometry and adjustable lamella slit spacing, enabling efficient lift-out and precise reattachment of variable-sized tissue volumes to pre-milled grids. The procedure is applicable across a range of biological tissues and is compatible with integrated cryo-correlative light and electron microscopy (cryo-CLEM) pipelines. By enhancing structural preservation and simplifying operational steps, this protocol provides a robust, reproducible framework to facilitate high-throughput, in situ structural analysis of tissues by cryo-ET.
Experimental study
Not applicable
Step-by-step procedure for an optimized serial lift-out cryo-focused ion beam milling technique in tissue analysis
1-Jan-2026