CELLestial™ Assay Kits for Live Cell Analysis Catalog
MitoToxicity
GPCRs
Nuclear Dynamics
Lysosomal Degradation
All CELLestial® dyes and probes
Apoptosis & Necrosis
Calcium Mobilization
Cell Cycle
ROS/RNS
Organelles
Apoptosis & Necrosis
Calcium Mobilization
Cell Cycle
Cytotoxicity
Organelles
MDR
ROS/RNS
The CELLestial® product line provides a variety of tools to help pharmaceutical and biotech companies optimize their pre-clinical and clinical drug development programs through early lead drug identification, lead candidate selection, predictive toxicology and compound characterization. Overall, these assays may be broadly classified into six main categories:
Cell-based assays for monitoring compound effects on apoptosis, autophagy and necrosis. Includes monitoring of annexin V redistribution, nuclear condensation, autophagosome generation and loss of plasma membrane integrity.
Cell-based assays for monitoring compound effects on reactive oxygen species, superoxide, nitric oxide and peroxynitrite.
Cell-based assays for monitoring compound effects on cell cycle dynamics, ribosome biogenesis, inhibition of transcription
Cell-based assays for monitoring compound effects on the function and viability of human cell lines. Includes monitoring cell viability, cell proliferation/cytotoxicity, lysosome expansion and mitochondrial activity.
Drugs targeting members of the G protein-coupled receptor (GPCR) super-family account for ~ 40% of all prescription pharmaceuticals on the market today. Calcium assays measure transient calcium mobilization for intracellular stores in response to the activation of Gαq-coupled GPCRs.
Multidrug resistance relates to resistance of tumor cells to a complete range of chemotherapy drugs with different structures and cellular targets. The phenomenon of multidrug resistance (MDR) is a well-known problem in oncology which necessitates a profound consideration in cancer treatment. The multidrug resistance kits provide fast, sensitive and quantitative method for monitoring the function and expression of the three clinically most important multidrug resistance proteins: MDR1 (P-glycoprotein), MRP1/2 and BCRP.