EdU Imaging Kits (HF594)
Measuring cell proliferation and cell cycle are a fundamental method to assess cell health, determine genotoxicity, and evaluate drug’s pharmacodynamic effect. The common method is measuring DNA synthesis directly. In previous experiments, there are several approaches such as the incorporation of radioactive nucleosides (3H-thymidine) or BrdU. Here, we introduce one new method, click chemistry-CuAAC (Copper-Catalyzed Azide-Alkyne Cycloaddition), and the use of this reaction in direct measurement of S-phase DNA synthesis in cell cycle.
A nucleoside analog of thymidine, EdU (5-ethynyl-2’-deoxyuridine), can be incorporated into DNA strand during DNA synthesis. The alkynyl group of EdU is a biologically inert group that will undergo an extremely selective reaction with dye’s azido via a CuAAC reaction to afford an 1,2,3-triazole product. EdU and HyperFluor™ 594 azide possess biologically unique moieties to label DNA of proliferating cells, producing low backgrounds and high detection sensitivities. This CuAAC reaction affords superior regioselectivity and quantitative transformation under extremely mild conditions.
EdU Imaging Kits (HF594) specifically labels the DNA of proliferating cells after HyperFluor™ 594 azide is ligated to EdU, then the proliferating cells can be detected by a microscope or flow cytometry.


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| Components | 50-500 Tests | |
| EdU (Component A) | 5 mg | |
| HyperFluor™ 594 azide (Component B) | 1 vial | |
| DMSO (Component C) | 4 mL | |
| 10X EdU Reaction Buffer (Component D) | 4 mL | |
| CuSO4 (100 mM Aqueous Solution) (Component E) | 1 vial | |
| EdU Buffer Additive (Component F) | 400 mg | |
| Hoechst 33342 (10 mg/mL in Water) (Component G) | 35 μL | |
Store at -20ºC, keep dry and protected from light, stable for 1 year. | ||







