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Annexin 5 fitc

Manufactured by Wanlei
Sourced in China

Annexin V-FITC is a fluorescently labeled protein that binds to phosphatidylserine, a molecule that is exposed on the surface of apoptotic cells. It is commonly used in flow cytometry and other analytical techniques to detect and quantify apoptotic cells.

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4 protocols using annexin 5 fitc

1

Annexin V-FITC and Propidium Iodide Apoptosis Assay

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Treated cells were collected by centrifugation, and the supernatant was discarded. The cells were washed twice with PBS and resuspended in 500 μl Binding Buffer (Wanleibio Co., Ltd., Shenyang, China). Next, 5 μL Annexin V-FITC (Wanleibio Co., Ltd.) and 10 μL propidium iodide (Wanleibio Co., Ltd.) were added and samples were mixed. Samples were incubated at room temperature away from light for 5-15 min. Analysis by flow cytometry was then performed.
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2

Apoptosis Quantification by Flow Cytometry

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After 24 h of treatment, the cells were collected and washed twice with PBS. The supernatant was removed and cells were re-suspended by the binding buffer. Five microliters of Annexin V-FITC (Wanleibio, Shenyang, China) and 10 μL of PI were added, and cells were incubated at room temperature for half an hour in the dark. The fluorescence was determined by flow cytometric analysis (Beckman-Coulter, Miami, FL, USA).
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3

Apoptosis Detection by Flow Cytometry

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The cells were collected and ltered through a 40-μm nylon cell strainer. The cells were washed with PBS and resuspended in binding buffer with Annexin V-FITC (Wanleibio, China) and Propidium Iodide (Wanleibio) at 4℃ for 15min and acquired on a FACS on CytoFLEX S (BECKMAN COULTER, USA). Data were analyzed using software (CytExpert 2.3).
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4

Apoptosis Quantification in Cell Lines

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In brief, the cells were inoculated in 6-well plates at a density of 2 × 103 per well. ZDQ-0620, GSK2126458 or DMSO were treated for 48 h, and the collected cells were stained in the dark with Annexin V-FITC and PI (Wanlei, China) for 10-20 min. Finally, the cells were sorted and quantitatively analyzed by flow cytometry (Becton-Dickinson, NJ, USA).
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