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Click it edu alexa fluor 488 cell proliferation kit for imaging

Manufactured by Thermo Fisher Scientific

The Click-iT EdU Alexa Fluor 488 Cell Proliferation Kit for Imaging is a fluorescent-based assay designed to detect and quantify cell proliferation. It utilizes a thymidine analog, EdU (5-ethynyl-2'-deoxyuridine), which is incorporated into newly synthesized DNA during the S phase of the cell cycle. The incorporated EdU is then detected using a fluorescent Alexa Fluor 488 dye, allowing for the visualization and quantification of proliferating cells.

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2 protocols using click it edu alexa fluor 488 cell proliferation kit for imaging

1

Extracellular Vesicle Imaging Workflow

Check if the same lab product or an alternative is used in the 5 most similar protocols
Click-iT EdU labeling was conducted using the Click-iT EdU Alexa Fluor 488 Cell Proliferation Kit for Imaging (ThermoFisher) according to manufacturer’s instructions. Following 60-minute incubation with EdU label, cells were washed extensively and the media replaced with EV-free complete cell culture media to allow for TMV shedding. TMVs were isolated as described above, and plated on poly-L-lysine coated coverslips for imaging. Cells and TMVs were fixed and subjected to Click-iT reaction according to manufacturer’s recommended protocol before staining with primary and secondary antibodies as described above.
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2

Extracellular Vesicle Imaging Workflow

Check if the same lab product or an alternative is used in the 5 most similar protocols
Click-iT EdU labeling was conducted using the Click-iT EdU Alexa Fluor 488 Cell Proliferation Kit for Imaging (ThermoFisher) according to manufacturer’s instructions. Following 60-minute incubation with EdU label, cells were washed extensively and the media replaced with EV-free complete cell culture media to allow for TMV shedding. TMVs were isolated as described above, and plated on poly-L-lysine coated coverslips for imaging. Cells and TMVs were fixed and subjected to Click-iT reaction according to manufacturer’s recommended protocol before staining with primary and secondary antibodies as described above.
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