Apoptosis

Monitor programmed cell death from membrane to nucleus

Of the three major established programmed cell death (PCD) pathways, Apoptosis (PCD Type 1) is the most-well characterized, being recognized as a critical regulator of development, immunity, as well as organ and tissue homeostasis. Apoptotic cells die in a controlled fashion in response to a variety of extrinsic or intrinsic signals (e.g., activation of TNF receptors, DNA damage, mitochondrial pathways). Influencing cells to undergo or resist apoptosis is the aim of countless drugs (both in use and development) for treatment of cancer, neurodegenerative, and immune-related disease. The interplay between apoptotic, autophagic, and necrotic pathways promises to yield further targets for therapeutic intervention. With over 400 products for the analysis of cell death, Enzo enables detection of phenotypic hallmarks of apoptotic cell death (see figure below), and the complete analysis of cross-talk between PCD pathways.


SuperFas Ligand
SuperKiller TRAIL
TNFα Protein, Antibodies & ELISAs
TNFR Protein, Antibodies & ELISAs



Death Receptor Ligands

Members of the tumor necrosis factor (TNF) receptor gene superfamily bind to extrinsic ligands and transduce intracellular signals leading to the destruction of the cell. Ligands, such as FasL and TNF-alpha, hold potential as targets for therapeutic and diagnostic applications.

Oligomerization Domains in Enzo Enhanced Ligands:
MEGA® Ligands – use the ACRP30headless domain from human or mouse ACRP30
KILLER® Ligands – use a KILLER® linker peptide that promotes trimerization
SUPERKILLER® Ligands – use the KILLER® linker peptide mutated to increase disulfide-mediated cross-linking


High-Throughtput Assays for Mitochondrial Function

A real-time mitochondrial membrane potential assay with superior sensitivity

    • More sensitive than JC-1
    • True mix-and-read homogeneous assay for live cells
    • Validated for multiple detection platforms: microscopy, flow cytometry, and microplates

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Apoptosis

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