Cellular assays, or cell-based assays, can be used in both biomedical research and drug-discovery screening applications to efficiently quantify cytotoxicity, biological activity, biochemical mechanisms and off-target interactions. The advantages of cell-based assays include the facilitation and generation of complex and biologically relevant data. Unlike traditional biochemical assays, cell-based assays are more physiologically relevant and can assess compound characteristics simultaneously.
Cell viability and proliferation assays can be effectively used to evaluate cell health. Cell viability and proliferation rate are often assessed using dyes such as trypan blue or Calcein-AM, or with fluorescent readouts. These assays may be used to quantify and to assess the health of mammalian cell lines, primary cells and stem cells.
Cell migration is the movement of cells in response to specific external signals, including chemical and mechanical stimuli. During cell invasion, cells can modulate the environment as they migrate through the structure of the extracellular matrix (ECM).
Cell migration and invasion can be evaluated in vitro with widely-used membrane-based migration systems such as the Boyden Chamber assay. Cell migration and invasion kits are oftenn used in cancer research to study cell motility and invasiveness in response to chemoattractant gradients.
Angiogenesis is the formation of blood vessels from existing vasculature and is controlled by chemical signals. Angiogenesis assays can be used to study both the induction and inhibition of angiogenesis in in vitro cell models. Cell-based assay development for drug discovery can accelerate optimization of treatments for cancer and other angiogenesis-dependent diseases.
Reactive oxygen species (ROS) are chemically reactive, oxygen-containing molecules. ROS assays can be used to screen chemical compounds and detect or better understand the effects of these species on mammalian cells. Cell-based ROS and oxidative stress assays provide biologically relevant information to assess cell viability, proliferation, or cytotoxicity as opposed to the binding or activity of biological molecules, one of the key differences in cell-based assays vs biochemical assays.
Protein assays are used to quantify protein concentration. Common protein assays include the enzyme-linked immunosorbent assay (ELISA), used to detect and quantify soluble substances for diagnostic purposes and quality control, and the MTT assay, used to measure cellular metabolic activity as an indicator of cell viability, proliferation and cytotoxicity.
Live cell analysis can be used to quantitatively measure cellular behavior over time, and to understand the influence of environmental cues. Advanced live cell analysis systems can provide necessary and unique insights into dynamic living processes. This unique insight is achieved microfluidic and other environmental-control live cell analysis chambers that control of gas, temperature, media changes to enable observation of cellular behavior. These instruments are augmented by non-cytotoxic, photostable dyes and fluorophores such as cell tracking dyes and fluorescent biosensors. Photostable media can enhance the stability of fluorescent trackers over long-term imaging studies.
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