Invitrogen™ Apo-Direct Apoptosis Detection Kit

Description

The APO-DIRECT™ Apoptosis Detection Kit includes sufficient reagents to process a total of 50 cell suspensions, including:

• 5mL positive and 5 mL negative control cell suspensions of approximately 1×10⁶ cells per mL in 70% (v/v) ethanol for assessing reagent performance
• Washing, reaction and rinsing buffers for processing individual steps in the assay
• Terminal deoxynucleotidyl transferase enzyme (TdT), Fluorescein-deoxyuridine triphosphate and propidium iodide/RNase A solution for counterstaining the total DNA

One of the most easily measured features of apoptotic cells is the break-up of the genomic DNA by cellular nucleases. These DNA fragments can be extracted from apoptotic cells and result in the appearance of DNA laddering when the DNA is analyzed by agarose gel electrophoresis. The DNA of non-apoptotic cells that remains largely intact does not display this laddering on agarose gels during electrophoresis.

The large number of DNA fragments appearing in apoptotic cells results in a multitude of 3′-hydroxyl termini in the DNA. This property can be used to identify apoptotic cells by labeling the 3′-hydroxyl ends with directly conjugated fluorescein- deoxyuridine triphosphate nucleotides (FITC-dUTP). The enzyme terminal deoxynucleotidyl transferase (TdT) catalyzes a template-independent addition of deoxyribonucleoside triphosphates to the 3′-hydroxyl ends of double- or single-stranded DNA with either blunt, recessed or overhanging ends. A substantial number of these sites are available in apoptotic cells providing the basis for the method utilized in the APO-DIRECT™ Kit. Non-apoptotic cells do not incorporate significant amounts of the FITC-dUTP due to the lack of exposed 3′-hydroxyl DNA ends.