Cell Cycle Assay Kit (Red Fluorescence)

FNCK113

20T/50T/100T

RNase A Reagent should be stored for 1 year at -20°C. PI Reagent should be stored at 2-8°C away from light for 1 year.

Cell Cycle Assay Kit (Red Fluorescence) is a kit that detects cell cycle by detecting DNA content. This kit can be used to detect the DNA content (cell cycle) of suspended or adherent cells.

Cell cycle refers to the whole process from the end of one mitosis to the end of the next. During this process, the genetic material is replicated and doubled, and evenly distributed to two daughter cells at the end of division. Cell cycle can be divided into phases like interphase and Metaphase. Intercellular phase can also be divided into dormancy (zero gap, G0), prophase of DNA synthesis (first gap, G1), anaphase of DNA synthesis (synthesis, S) and anaphase of DNA synthesis (second gap, G2). DNA can bind to some specific fluorescent dyes (such as propidium Iodide-PI), the fluorescent dyes binding to DNA at different stages are different, and the fluorescence intensity detected by flow cytometry can also be used to detect different phases in cell cycle.

After staining with PI, assuming that the fluorescence intensity of G0/G1 phase cells is 1, the theoretical value of fluorescence intensity of G2/M phase cells containing double genomic DNA is 2, and the fluorescence intensity of S phase cells undergoing DNA replication is between 1 and 2. Apoptotic cells lost part of genomic DNA fragmentation due to nucleus concentration and DNA fragmentation. Therefore, apoptotic cells showed obvious weak staining after PI staining and the fluorescence intensity was less than 1. The sub-G1 peak appeared on the flow cytometry result which is apoptotic cell.

The following figure shows the cell cycle results of Jurkat cells after treated with 70% ethanol overnight with this kit:

1． Reagent Preparation

A．Store the absolute ethanol at -20°C overnight.

B．Take out the RNase A reagent dissolve fully, mix it and put on ice for use.

2． Sample Preparation

1） Collect 5×105 cells for each, centrifuge at 300×g for 5 min and discard the supernatant. Add 1 mL PBS to resuspend gently and count the cells.

2） Centrifuge at 300×g for 5 min and discard the supernatant.

3） Add 0.3 mL PBS to resuspend the cells.

3． Add 0.7 mL absolute ethanol from -20°C refrigerator, mix fully and store at -20°C for 1 h or overnight.

4． Centrifuge at 300×g for 5 min and discard the supernatant. Add 1 mL PBS to resuspend the cells, store at RT for 15 min.

5． Centrifuge at 300×g for 5 min and discard the supernatant. Add 100 μL RNase A reagent to resuspend the cells, incubate at 37°C water bath for 30 min.

6． Add 400 μL PI Reagent, mix fully and incubate at 2-8°C for 30 min in the dark.

7． Analyze the cells immediately with proper machine settings.

1.For maximal assay performance, this kit should be used within 12 months. Avoid freeze/thaw cycles.

2.The experimental results need to be detected by flow cytometer.

3.Detect apoptosis as soon as possible after staining to avoid increase in apoptosis or necrosis.

4.Avoid extended exposure of the samples to direct light to protect the fluorophores from quenching.

5.For your safety and health, please wear a lab coat and disposable gloves.

6.This kit is for scientific research only.