The largest database of trusted experimental protocols

Annexin 5 fitc apoptosis detection kit

Manufactured by Boster Bio
Sourced in China

The Annexin V-FITC apoptosis detection kit is a laboratory tool used to detect and quantify apoptosis, a type of programmed cell death. The kit utilizes Annexin V, a protein that binds to phosphatidylserine, a molecule exposed on the surface of cells undergoing apoptosis. The Annexin V is labeled with the fluorescent dye FITC, allowing for the visualization and analysis of apoptotic cells using flow cytometry or fluorescence microscopy.

Automatically generated - may contain errors

3 protocols using annexin 5 fitc apoptosis detection kit

1

Apoptosis Assay of AMTB Treated Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
After treating cells with different concentrations of AMTB (0 μM, 10 μM, 20 μM, 30 μM) for 24 h. Cell apoptosis was detected using Annexin V-FITC apoptosis detection kit (Boster Biological Technology Co., Ltd., California, USA) in accordance with the manufacturer’s instructions. Specimens were analyzed with BD FACS Calibur (Beckman Coulter, CA, USA) and the apoptotic rate was determined by the FlowJo software (Tree Star Inc., Ashland, USA). Each experiment was independently repeated for three times.
+ Open protocol
+ Expand
2

Apoptosis Induction by T4O in PC Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
After 24 h, PC cells were seeded in six-well plates and treated with different concentrations (0, 0.5, 1, and 2 μM) of T4O. After washing three times with PBS, the cells were stained using the Annexin V-FITC Apoptosis Detection Kit (Boster, Wuhan, China) and then detected using a DeFLEX flow cytometer (Beckman, USA). The results were analyzed using Flwo JO.
+ Open protocol
+ Expand
3

Apoptosis Detection in HUVEC and MCF-7 Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
ERa-positive HUVEC and MCF-7 cells were separately seeded on 6-well plates with 4 Â 10 3 cells per well. After 24 h, cells were treated with formononetin for 48 h, collected, and then washed three times using ice-cold PBS. Cells were stained with Annexin Vfluorescein isothiocyanate (FITC) and propidium iodide (PI) for 30 min in the dark at room temperature in 500 mL of binding buffer. Under a FACS Aria flow cytometer (Becton Dickinson), nonstained cells were viable, and cells stained with Annexin V were judged at the early stage of apoptosis. Surface exposure of phosphatidylserine in apoptotic cells was measured using an Annexin V-FITC apoptosis detection kit (Boster, Hubei, China), according to the manufacturer's instructions. Additional exposure to PI made it possible to differentiate the early apoptosis cells
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!