Cell Cycle Assay Kit (Red Fluorescence)
Introduction
Elabscience Cell Cycle Assay Kit (Fluorometric-Red) is a kit that detects cell cycle by detecting DNA content.Cell cycle refers to the whole process from the end of one mitosis to the end of the next. During this process, thegenetic material is replicated and doubled, and evenly distributed to two daughter cells at the end of division. Cellcycle 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 anaphaseof 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 flowcytometry 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 offluorescence intensity of G2/M phase cells containing double genomic DNA is 2, and the fluorescence intensity of Sphase cells undergoing DNA replication is between 1 and 2. Apoptotic cells lost part of genomic DNA fragmentationdue to nucleus concentration and DNA fragmentation. Therefore, apoptotic cells showed obvious weak staining afterPI staining and the fluorescence intensity was less than 1. The sub-G1 peak appeared on the flow cytometry resultwhich is apoptotic cell. The kit can be used to detect the DNA content (cell cycle) of cultured cells (suspension or adherence cells).
Molt-4 cells were treated with 70%ethanol overnight and detected withthis kit.
Product Details
Properties
| Application | Cell Cycle |
| Detection method | Fluorometric Method |
| Sample type | Cell samples |
| Assay time | 3 hours |
| Detection instrument | Flow Cytometer |
| Dye Type | PI |
| Ex/Em (nm) | 536/617 |
| Channel set | PI,PerCP,PE |
| Other reagents required | Ethanol, PBS(E-IR-R187) |
| Storage | 2~8C/-20C, shading light. Refer to the Manual. |
| Shipping | Ice bag |
| Expiration date | 12 months |
Staining Procedure
- Reagent Preparation
A. Store the absolute ethanol at -20C overnight.
B. Take out the RNase A reagent dissolve fully, mix it and put on ice for use. - Sample Preparation
1) Collect 5105 cells for each, centrifuge at 300g for 5 min and discard the supernatant. Add PBS toresuspend gently and count the cells.
2) Centrifuge at 300g for 5 min and discard the supernatant.
3) Add 0.3 mL PBS to resuspend the cells. - Add 1.2 mL absolute ethanol from -20C refrigerator, mix fully and store at -20C for 1 h or overnight.
- Centrifuge at 300g for 5 min and discard the supernatant. Add 1 mL PBS to resuspend the cells, store at RT for 15 min.
- Centrifuge at 300g for 5 min and discard the supernatant. Add 100 L RNase A reagent to resuspend the cells, incubate at 37C water bath for 30 min.
- Add 400 L PI Reagent (50g/mL), mix fully and incubate at 2-8C for 30 min in the dark.
- Analyze the cells immediately with proper machine settings.
Storage
RNase A Reagent should be stored at -20C. PI Reagent (50g/mL) should be stored at 2~8C in dark.
Notes
- For maximal assay performance, this kit should be used within 12 months. Avoid freeze/thaw cycles.
- The experimental results need to be detected by flow cytometer.
- Detect apoptosis as soon as possible after staining to avoid increase in apoptosis or necrosis.
- Avoid extended exposure of the samples to direct light to protect the fluorophores from quenching.
- This kit is for research use only. For your safety and health, please wear lab clothes and gloves. Instructions should be followed strictly, changes of operation may result in unreliable results.
