Annexin V-FITC/PI apoptosis assay kit
Annexin V-FITC/PI apoptosis assay kit
Packing specification
Product number: An0020, An0050, An0100
Specifications: 20T, 50T, 100T
Storage conditions
Stored at 4oC, valid for one year
Product Description
The Annexin V-FITC Apoptosis assay kit detects apoptotic cells by flow cytometry. The annexins are a group of homologous proteins which bind phospholipids in the presence of calcium. Annexin V-FITC is a fluorescent probe which binds to phosphatidylserine in the presence of calcium. Apoptosis, or programmed cell death, is a mechanism of cells used to negatively select cells that are deleterious to the host. The cellular changes involved in the process include loss of phospholipid asymmetry during the early stages of apoptosis. In living cells, phosphatidylserine is transported to the inside of the lipid bilayer by the Mg-ATP dependent enzyme, aminophospholipid translocase. At the onset of apoptosis, phosphatidyl- serine, which is normally found on the internal part of the plasma membrane, becomes translocated to the external portion of the membrane. The phosphatidyl- serine becomes available to bind to the annexin V-FITC conjugate in the presence of calcium.
The procedure consists of the binding of annexin V- FITC to phosphatidylserine in the membrane of cells, which are beginning the apoptotic process, and the binding of propidium iodide to the cellular DNA in cells where the cell membrane has been totally compromised. Apoptosis may be either spontaneous or induced by incubating the cells with staurosporine. The cells are incubated with annexin V-FITC and propidium iodide. After a 10 minute incubation period at room temperature the cells are analyzed by flow cytometry. Annexin V-FITC is detected as a green fluorescence and propidium iodide is detected as a red fluorescence.
Reagents:
|
Reagents |
20 assays |
50 assays |
100 assays |
Storage |
|
Annexin V-FITC product code:FI001 |
100 μl |
250 μl |
500 μl |
4°C in the dark |
|
Propidium Iodide, PI product code:PI002 |
200 μl |
500 μl |
1000 μl |
4°C in the dark |
|
Binding Buffer ( 4′ ) product code:BU002 |
4 ml |
10 ml |
20 ml |
4°C |
Precautions and Disclaimer
This product is for R&D use only, not for drug, household, or other uses. Annexin V is a product of human origin; handle as if capable of transmitting infectious agents.
Preparation Instructions
Allow all kit components to reach room temperature before use.
Dilute the Binding Buffer 1:4 with deionized water (4ml Binding Buffer+12ml deionized water).
Dissolve the staurosporine in DMSO to a concentration of 100 μg/ml.
Procedure
This procedure describes the induction of apoptosis in the Jurkat cell line, followed by measurement of phosphatidylserine. Perform the experiment using aseptic technique.
1. Induce apoptosis in a 1 x 106 cells/ml suspension of Jurkat cells by the addition of 1 μg/ml staurosporine.
2. Establish a control of non-induced Jurkat cells at 1 x 106 cells/ml for a zero time data point.
3. Incubate both Jurkat cell cultures for 1–2 hours in a 37 °C, 5% CO2 incubator.
4. Wash the cells twice with DPBS.
5. Resuspend the cells in 1× Binding Buffer at a concentration of ~1 x 106 cells/ml.
6. Add 500 μl of the apoptotic cell suspension to a plastic 12 × 75 mm test tube.
7. Add 500 μl of the non-induced cell suspension to a second plastic 12 × 75 mm test tube.
8. Add 5 μl of Annexin V FITC Conjugate and 10 μl of Propidium Iodide Solution to each cell suspension.
9. Incubate the tubes at room temperature for exactly 10 minutes and protect from light.
10. Determine the fluorescence of the cells immediately with a flow cytometer. Cells, which are early in the apoptotic process, will stain with the Annexin V FITC Conjugate alone. Live cells will show no staining by either the Propidium Iodide Solution or Annexin V FITC Conjugate. Necrotic cells will be stained by both the Propidium Iodide Solution and Annexin V FITC Conjugate.
