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Electric cell-substrate impedance sensing

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current pathways through and around the cell bodies change as well, leading to a corresponding increase or decrease of impedance. Thus, by recording time-resolved impedance measurements, cell shape changes can be followed in real time with sub-microscopic resolution and can be used for bioanalytic purposes.
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particles so that the impedance increases with increasing coverage of the electrode until a confluent (i.e. continuous) layer of cells is established. In confluent cell layers the measured impedance is mainly determined by the three-dimensional shape of the cells. If cell shape changes occur, the
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as well as chemical, biological or physical stimuli, the ECIS technique is applied in various experimental settings in cell biological research laboratories. It can be used as a
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Wegener, Keese, Giaever: ECIS as a non-invasive means to follow the kinetics of cell spreading on artificial surfaces.
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of the cell-covered electrode is then measured at one or several frequencies as a function of time. Due to the
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activity of adherent cells spread on the electrode surface (micromotion) as well as their
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Wegener, Zink, Roesen, Galla: Use of electrochemical impedance measurements to monitor
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surfaces. Equipments based on the ECIS technique are also dedicated to monitor the
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As the shape of animal cells responds very sensitively to alterations in
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In ECIS the cells are grown on the surface of small and planar gold-film
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Giaever & Keese: A morphological biosensor for mammalian cells,
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or as a non-invasive means to follow cell adhesion to
36:, i.e. within a well-defined laboratory environment. 23:(a trademark of Applied BioPhysics Inc.) refers to a 131:stimulation of bovine aortic endothelial cells. 27:biophysical approach to monitor living animal 8: 17:Electric cell-substrate impedance sensing 107: 7: 14: 1: 197: 95:activities in ECIS-based 59:the cells behave like 181:Laboratory techniques 55:properties of their 135:437/6(1999)925-934 188: 176:Research methods 161:Microphysiometry 149: 148:259(2000)158-166 142: 136: 133:Eur. J. Physiol. 125: 119: 112: 81:drug development 196: 195: 191: 190: 189: 187: 186: 185: 166: 165: 157: 152: 143: 139: 126: 122: 113: 109: 105: 12: 11: 5: 194: 192: 184: 183: 178: 168: 167: 164: 163: 156: 153: 151: 150: 146:Exp. Cell Res. 137: 120: 118:366(1993)591-2 106: 104: 101: 13: 10: 9: 6: 4: 3: 2: 193: 182: 179: 177: 174: 173: 171: 162: 159: 158: 154: 147: 141: 138: 134: 130: 124: 121: 117: 111: 108: 102: 100: 98: 97:wound healing 94: 90: 86: 82: 78: 74: 70: 65: 62: 58: 54: 50: 46: 42: 37: 35: 34: 30: 26: 22: 18: 145: 140: 132: 129:b-adrenergic 123: 115: 110: 89:chemokinetic 84: 77:cytotoxicity 66: 38: 31: 25:non-invasive 20: 16: 15: 93:chemotactic 170:Categories 103:References 69:metabolism 61:dielectric 53:insulating 47:). The AC 45:Petri dish 41:electrodes 79:studies, 57:membranes 49:impedance 155:See also 99:assays. 85:in vitro 33:in vitro 116:Nature 73:sensor 29:cells 21:ECIS 75:in 19:or 172::

Index

non-invasive
cells
in vitro
electrodes
Petri dish
impedance
insulating
membranes
dielectric
metabolism
sensor
cytotoxicity
drug development
chemokinetic
chemotactic
wound healing
b-adrenergic
Microphysiometry
Categories
Research methods
Laboratory techniques

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