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Cat.No.:E-CK-A322
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When cells undergo apoptosis, specific DNA endonucleases will be activated, cutting the genomic DNA between the nucleosomes. The DNA of apoptotic cells is cleaved into multimers of 180~200bp fragments, corresponding to the oligonucleosomal size. Therefore, the DNA of apoptotic cells typically migrates as a ladder of 180~200bp on an agarose gel. The exposed 3'-OH of the broken DNA can be catalyzed by Terminal Deoxynucleotidyl Transferase (TdT) with fluorescein labeled dUTP, which can be detected with fluorescence microscope.
Application | DNA Fragmentation |
Detection method | Fluorometric Method |
Sample type | Paraffin section, frozen section, cell slide |
Assay time | 3 hours |
Detection instrument | Fluorescence Microscope |
Dye Type | Elab Fluor® 594 |
Ex/Em (nm) | 590/617 |
Filter set | TRITC |
Other reagents required | 4% Paraformaldehyde(E-IR-R113),0.2% Triton X-100(E-IR-R122),PBS(E-IR-R187),ddH2O,Mounting solution with anti-fluorescence quencher(E-IR-R119),Xylene,Ethanol |
Storage | -20°C, shading light |
Shipping | Ice bag |
Expiration date | 12 months |
Sample: Tissue Slice |
PMID: 34788107 |
Sample: Sputum |
PMID: 35883161 |
PMID: 36195952 |
PMID: 36333308 |
PMID: 36787636 |