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제품 설명
Elab Fluor® 555-11-dUTP
제품 번호
E-CK-A125D
제품 특징
Detection principle
Chromosome DNA breakage is an important marker event in cell apoptosis. A series of DNA 3'-OH terminus is produced by DNA double-strand breaks in apoptotic cells or whenever there is a gap in one strand. The fluorescen labeled dUTP can be linked to the 3' -OH terminus of the broken DNA under the action of terminal deoxyribonucleotide transferase (TdT). Fluorescence of dUTP conjugate can be detected by flow cytometer or fluorescence microscope.
Application | DNA Fragmentation |
Detection method | Fluorometric Method |
Sample type | Paraffin section, frozen section, cell slide |
Detection instrument | Fluorescence Microscope |
Dye Type | Elab Fluor® 555 |
Ex/Em (nm) | 555/565 |
Filter set | TRITC |
Storage | -20°C, shading light |
Shipping | Ice bag |
Expiration date | 12 months |
E-CK-A211 | Annexin V-FITC/PI Apoptosis Kit |
E-CK-A301 | Mitochondrial Membrane Potential Assay Kit (with JC-1) |
E-CK-A362 | Enhanced Cell Counting Kit 8 (WST-8/CCK8) |
Data Image
Hela cells was treated with DNase I to fragment the DNA. DNA strand breaks showed intense fluorescent staining in DNase I treated sample.(Red)
Paraffin embedded mouse colon was treated with DNase I to fragment the DNA. DNA strand breaks showed intense fluorescent staining in DNase I treated sample (red).
Mixed samples of normal mouse spleen cells and DNase I treated mouse spleen cells were stained.
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