Annexin V-iFluor 488 Apoptosis Staining / Detection Reagent (ab219904) is a cell-impermeable reagent designed to bind to phosphatidylserine (PS) residues exposed on the outer cell surface of cells with a flow cytometer or fluorescence microscopy at Ex/Em = 494/520 nm.
Fluorescent
Suspension cells, Adherent cells
Quantitative
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This protein is an anticoagulant protein that acts as an indirect inhibitor of the thromboplastin-specific complex, which is involved in the blood coagulation cascade.
Annexin A5, Anchorin CII, Annexin V, Annexin-5, Calphobindin I, Endonexin II, Lipocortin V, Placental anticoagulant protein 4, Placental anticoagulant protein I, Thromboplastin inhibitor, Vascular anticoagulant-alpha, CBP-I, PP4, PAP-I, VAC-alpha, ANXA5, ANX5, ENX2, PP4
Annexin V-iFluor 488 Apoptosis Staining / Detection Reagent (ab219904) is a cell-impermeable reagent designed to bind to phosphatidylserine (PS) residues exposed on the outer cell surface of cells with a flow cytometer or fluorescence microscopy at Ex/Em = 494/520 nm.
Fluorescent
Suspension cells, Adherent cells
Quantitative
Flow cytometer
Blue Ice
-20°C
-20°C
-20°C
Annexin V-iFluor 488 Apoptosis Staining / Detection Reagent (ab219904) is a cell-impermeable reagent designed to bind to phosphatidylserine (PS) residues exposed on the outer cell surface of cells with a flow cytometer or fluorescence microscopy at Ex/Em = 494/520 nm.
We recommend using an impermeable nuclear stain such as Propidium Iodide (Annexin V/ANXA5-FITC Apoptosis Detection Reagent (500X) ab14082) or DRAQ7™ (DRAQ7™ ab109202) together with Annexin V-iFluor 488 Detection Reagent to discriminate necrotic and dead cells: plasma membrane is disrupted in these cells and therefore the Annexin V reagent will bind to PS found in the interior of cells.
Apoptosis is a regulated process of cell death that occurs during embryonic development as well as maintenance of tissue homeostasis. Inappropriately regulated apoptosis is implicated in different disease states, such as neurodegeneration disease and cancer. The apoptosis program is characterized by morphologic features, including loss of plasma membrane asymmetry and attachment, condensation off the cytoplasm and nucleus, and compaction and fragmentation of the nuclear chromatin. Exposure of phosphatidylserine (PS) on the external surface of the cell membrane has been reported to occur in the early phases of apoptotic cell death, during which the cell membrane remains intact. In leukocyte apoptosis, PS on the outer surface of the cell marks the cell for recognition and phagocytosis by macrophages. The human vascular anticoagulant, annexin V, is a 35-36 kDa Ca2+ dependent phospholipid binding protein that has a high affinity for PS, and shows minimal binding to phosphatidylcholine and sphingomyelin. Changes in PS asymmetry, which can be analyzed by measuring annexin V binding to the cell membrane, are generally observed before morphological changes associated with apoptosis occurred and before membrane integrity is lost.
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The detection of binding activity of Annexin V-mFluor Violet 450 Apoptosis Staining / Detection Reagent ab219911.
Annexin V-iFluor 488 Detection Reagent (ab219904) Detection of phosphatidylserine (PS) exposure in Jurkat cells. Jurkat cells were left untreated (blue) or treated with 20 μM camptothecin (red) in a 37°C, 5% CO2 incubator for 4-5 hours. Cells were then incubated with Annexin V-iFluor reagent and PI for 30 minutes. The fluorescence intensitiy of Annexin V-iFluor 488 was measured with a FACSCalibur (BD Systems) flow cytometer using the FL1channel.
In live non-apoptotic cells, Annexin V-iFluor 488 conjugate detects innate apoptosis in non-induced cells, which is typically 2-6% of all cells. In apoptotic cells Annexin V-iFluor Violet488 conjugate binds to phosphatidylserine, which is located on the outer leaflet of the cell membrane, resulted in increased staining intensity.
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