Ca 2+ functions as an important intracellular signal for a wide range of cellular processes. These processes are selectively activated by controlled spatiotemporal dynamics of the free cytosolic Ca 2+ . Intracellular Ca 2+ dynamics are regulated by numerous cellular parameters. Here, we established a new way to determine neuronal Ca 2+ handling properties by combining the ‘added buffer’ approach (Neher and Augustine, 1992) with perforated patch-clamp recordings (Horn and Marty, 1988). Since the added buffer approach typically employs the standard whole-cell configuration for concentration-controlled Ca 2+ indicator loading, it only allows for the reliable estimation of the immobile fraction of intracellular Ca 2+ buffers. Furthermore, crucial components of intracellular signaling pathways are being washed out during prolonged whole-cell recordings, leading to cellular deterioration. By combining the added buffer approach with perforated patch-clamp recordings, these issues are circumvented, allowing the precise quantification of the cellular Ca 2+ handling properties, including immobile as well as mobile Ca 2+ buffers.