Immunogenicity is a powerful approach used in cell biology to visualize and analyse the dynamic behaviour of cells in real time. This technique allows researchers to observe cellular processes, such as cell division, migration, differentiation, and signalling, with high spatial and temporal resolution, providing insights into the underlying mechanisms governing cellular behaviour. Various imaging modalities are employed in Immunogenicity, including light microscopy, fluorescence microscopy, confocal microscopy, live-cell imaging, and super-resolution microscopy techniques. These methods enable researchers to visualize cellular structures, organelles, and molecular events within living cells, allowing for the dynamic monitoring of cellular processes in physiological conditions. Fluorescent protein markers, such as green fluorescent protein (GFP) and its variants, are commonly used in Immunogenicity to label specific proteins, organelles, or cellular structures of interest. By genetically encoding fluorescent tags into cells, researchers can track the localization, movement, and interactions of target molecules in real time, providing valuable insights into their dynamics and functions within living cells. Live-cell imaging techniques allow for the observation of cellular processes over extended periods, ranging from minutes to hours or even days, enabling the study of dynamic events such as cell migration, cell-cell interactions, and morphological changes during development or disease progression.
Title : AI-integrated high-throughput tissue-chip for space-based biomanufacturing applications
Kunal Mitra, Florida Tech, United States
Title : Will be updated soon...
Vasiliki E Kalodimou, European University-Cyprus Ltd, Cyprus
Title : Will be updated soon...
Nagy Habib, Imperial College London, United Kingdom
Title : Will be updated soon...
Alexander Seifalian, Nanotechnology & Regenerative Medicine Commercialisation Centre, United Kingdom
Title : Advanced 3D tissue models: Pioneering tools for investigating health and disease
Lucie Bacakova, Institute of Physiology of the Czech Academy of Sciences, Czech Republic
Title : Developing iPSC-derived 3D Outer Blood-Retinal Barrier Disease Models of Choroideremia for Gene Therapy Evaluation
Aradhana Kasimsetty, National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), United States