Annexin V is a phosphatidylserine (PS) binding protein which is used to detect PS on the surface of
cells undergoing apoptotis. Apoptosis or programmed cell death (PCD) is a genetically encoded cell
elimination program which ensures an equilibrium between cell proliferation and cell death and by
which damaged or unwanted cells are eliminated.
During the early stages of apoptosis, cells loose their phospholipid membrane symmetry and expose
phosphatidylserine at the cell surface while the plasma membrane remains intact. The exposure of
phosphatidylserine on the outside of the cell can be monitored in cell suspensions using fluorochrome
labelled Annexin V in flow cytometry (1,2,3)
Application:
Annexin V is used to detect apoptosis in cell suspensions by flow cytometry or immunofluorescence
microscopy. The ability to monitor cell death is important in a wide variety of clinical situations.
One of the frequent applications is monitoring cell death during tumor therapy. For example,
stimulation of apoptosis occurs when maligniancies are treated with cytotoxic drugs or ionizing
radiation and in psoriasis by UV radiation. Understanding alterations in the cell death program may
yield new approaches in therapy.
Cells may be programmed to die when they have lost growth regulation or experienced DNA damage due
to radiation or drug action. Similarly self-reactive T-cells and virus-infected cells recognized by
cytotoxic T-cells are all deleted to promote survival of the organism. The exposure of PS on the
outside of the cell membrane is a signal to the surrounding phagocytes to remove the dying cell from
the tissues. This exposure starts soon after the cell enters the apoptotic process, well before
nuclear condensation and DNA cleavage become visible.
Specifications:
Annexin V is a phospholipid binding protein which exhibits high affinity and selective binding to
phosphotidylserine in the presence of calcium ions. It is a highly specific marker of apoptosis.
References:
1. Koopman,G., et al 1994. Blood. 84, 1415-1420
2. Vermes,I., et al., 1995. J. Immunol. Methods, 180, 39-52
3. van Engeland, M., et al Cytometry, 1996. 24. 131-139
For research only. Not for use in humans. For in vitro use only