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This invention provides devices and apparatuses comprising the same, for the mixing and pumping of relatively small volumes of fluid. Such devices utilize nonlinear electrokinetics as a primary mechanism for driving fluid flow. Methods of cellular analysis and high-throughput, multi-step product for

This invention provides devices and apparatuses comprising the same, for the mixing and pumping of relatively small volumes of fluid. Such devices utilize nonlinear electrokinetics as a primary mechanism for driving fluid flow. Methods of cellular analysis and high-throughput, multi-step product formation using, devices of this invention are described.

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What is claimed is: 1. A microfluidic device comprising one or more inlet ports, one or more outlet ports and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps and one or more micromixers, wherein: said micropumps comprise a passageway for

What is claimed is: 1. A microfluidic device comprising one or more inlet ports, one or more outlet ports and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps and one or more micromixers, wherein: said micropumps comprise a passageway for transmitting an electrolyte fluid; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microchannel; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said at least one conductor element produce electro-osmotic flows so that said electrolyte fluid is driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting an electrolyte fluid; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microfluidic channel; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said conductor element produce electro-osmotic flows with varied trajectories, and said electrolyte fluid is driven across said microfluidic channels so that said electrolyte fluid is mixed in said microfluidic channels. 2. The microfluidic device of claim 1, wherein said conductor element is comprised of a symmetric cylinder of a defined radius. 3. The microfluidic device of claim 2, wherein said radius ranges from about 5 to about 250 μm. 4. The microfluidic device of claim 1, wherein said conductor element is comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section. 5. The microfluidic device of claim 4, wherein said conductor element is comprised of a conducting strip. 6. The microfluidic device of claim 5, wherein at least one wall of said microfluidic channels comprises said conducting strip. 7. The microfluidic device of claim 4, wherein the shape of said conductor element approximates an arrowhead, teardrop, or ellipse. 8. The microfluidic device of claim 1, wherein said microfluidic channels form a cross-junction, an elbow-junction, a T-junction, a Y-junction, or a combination thereof. 9. The microfluidic device of claim 1, wherein said conductor element is comprised of a symmetric conductor element. 10. The microfluidic device of claim 1, wherein said microfluidic channels are comprised of a transparent material. 11. The microfluidic device of claim 1, wherein said microfluidic channels are comprised of a metal. 12. The microfluidic device of claim 11, wherein said metal is a metal bilayer. 13. The microfluidic device of claim 12, wherein an exposed layer of said bilayer is functionalized to minimize adherence of material conveyed through said device. 14. The microfluidic device of claim 1, wherein said device comprises an array of conductor elements. 15. An apparatus comprising the microfluidic device of claim 1. 16. The microfluidic device from claim 1, wherein said device further comprises a center electrode. 17. A method of cellular analysis comprising the steps of: a. introducing a buffered suspension comprising cells to a first inlet port of a microfluidic device; b. introducing a reagent for cellular analysis to said first inlet or to a second inlet port of said microfluidic device, said microfluidic device comprising: one or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof wherein: a. said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microchannel; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said suspension and said reagent are driven across said microfluidic channels; and b. said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microfluidic channels; an array of conductor elements placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said suspension and said reagent are driven across said microfluidic channels so that said suspension and said reagent are mixed in said microfluidic channels; and analyzing at least one parameter affected by contact between said suspension and said reagent. 18. The method of claim 17, wherein said reagent is an antibody, a nucleic acid, an enzyme, a substrate, a ligand, or a combination thereof. 19. The method of claim 18, wherein said reagent is coupled to a detectable marker. 20. The method of claim 19, wherein said marker is a fluorescent compound. 21. The method of claim 20, wherein said device is coupled to a fluorimeter or fluorescent microscope. 22. The method of claim 21, wherein said device is comprised of a transparent material. 23. The method of claim 17, further comprising the step of introducing a cellular lysis agent in an inlet port of said device. 24. The method of claim 23, wherein said reagent specifically interacts or detects an intracellular compound. 25. A method of high-throughput, multi-step product formation, the method comprising the steps of: a. introducing a first liquid comprising a precursor to a first inlet port of a microfluidic device; b. introducing a second liquid comprising a reagent, catalyst, reactant, cofactor, or combination thereof to a second inlet port of said microfluidic device, said microfluidic device comprising: i. two or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof wherein: said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microchannel; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said first liquid and said second liquid are driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microfluidic channels; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said first liquid and said second liquid are driven across said microfluidic channels so that said first liquid and said second liquid are mixed in said microfluidic channels; and c. collecting said mixed liquid from an outlet port of said device. 26. The method of claim 25, further comprising carrying out iterative introductions of said second liquid, as in (b), to additional inlet ports. 27. The method of claim 25, wherein said reagent is an antibody, a nucleic acid, an enzyme, a substrate, a ligand, a reactant or a combination thereof 28. A method of drug processing and delivery, the method comprising the steps of: a. introducing a first liquid comprising a drug to a first inlet port of a microfluidic device; b. introducing a second liquid comprising a buffer, a catalyst, or combination thereof to said first inlet port or to a second inlet port of said microfluidic device, said microfluidic device comprising: i. two or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof wherein: said micropumps comprise a passageway for transmitting said first and said second liquids; a source providing an electric field in said microchannel; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said first liquid and said second liquid are driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting said first liquid and said second liquid; a source providing an electric field in said microfluidic channels; one or more conductor elements placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said first liquid and said second liquid are driven across said microfluidic channels so that said first liquid and said second liquid are mixed in said microfluidic channels; and c. delivering the product of (b) to a subject, through an outlet port of said device. 29. The method of claim 28, further comprising carrying out iterative introductions of said second liquid to said inlet ports. 30. The method of claim 28, wherein introduction of said second liquid serves to dilute said drug to a desired concentration. 31. A method of analyte detection or assay, comprising the steps of: a. introducing a fluid comprising an analyte to a first inlet port of a microfluidic device, said microfluidic device comprising: i. one or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps and one or more micromixers, wherein: a. said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microchannel; at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said suspension and said reagent are driven across said microfluidic channels; and b. said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microfluidic channels; an array of conductor elements placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said suspension and said reagent are driven across said microfluidic channels so that said suspension and said reagent are mixed in said microfluidic channels; c. said microchannels being coated with a reagent for the detection, assay, or combination thereof of said analyte; and detecting, analyzing, or a combination thereof, of said analyte. 32. The microfluidic device of claim 31, wherein said device further comprises a center electrode. 33. The microfluidic device of claim 31, wherein said device comprises obstacles in said channels, which impede or change fluid flow in said channels. 34. A microfluidic device comprising one or more inlet ports, one or more outlet ports and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof, wherein: said micropumps comprise a passageway for transmitting an electrolyte fluid; a source providing a DC electric field in said microchannel; at least one conductor element comprised of a symmetric cylinder of a defined radius that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said at least one conductor element produce electro-osmotic flows so that said electrolyte fluid is driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting an electrolyte fluid; a source providing a DC electric field in said microfluidic channel; at least one conductor element comprised of a symmetric cylinder of a defined radius that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said conductor element produce electro-osmotic flows with varied trajectories, and said electrolyte fluid is driven across said microfluidic channels so that said electrolyte fluid is mixed in said microfluidic channels. 35. The microfluidic device of claim 34, wherein said field source is comprised of electrodes of different polarities. 36. The microfluidic device of claim 34, wherein said radius ranges from about 5 to about 250 μm. 37. The microfluidic device of claim 34, wherein said microfluidic channels form a cross-junction, an elbow-junction, a T-junction, a Y-junction, or a combination thereof. 38. The microfluidic device of claim 34, wherein said microfluidic channels are comprised of a transparent material. 39. The microfluidic device of claim 35, wherein said microfluidic channels are comprised of a metal. 40. The microfluidic device of claim 39, wherein said metal is a metal bilayer. 41. The microfluidic device of claim 40, wherein an exposed layer of said bilayer is functionalized to minimize adherence of material conveyed through said device. 42. The microfluidic device of claim 34, wherein said device comprises an away of conductor elements. 43. An apparatus comprising the microfluidic device of claim 34. 44. A method of cellular analysis comprising the steps of: a. introducing a buffered suspension comprising cells to a first inlet port of a microfluidic device; b. introducing a reagent for cellular analysis to said first inlet or to a second inlet port of said microfluidic device, said microfluidic device comprising: i. one or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof, wherein: a. said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microchannel; at least one conductor element comprised of a symmetric cylinder of a defined radius that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said suspension and said reagent are driven across said microfluidic channels; and b. said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microfluidic channels; an anay of conductor elements comprised of symmetric cylinders of a defined radius placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said suspension and said reagent are driven across said microfluidic channels so that said suspension and said reagent are mixed in said microfluidic channels; and analyzing at least one parameter affected by contact between said suspension and said reagent. 45. The method of claim 44, wherein said reagent is an antibody, a nucleic acid, an enzyme, a substrate, a ligand, or a combination thereof 46. The method of claim 45, wherein said reagent is coupled to a detectable marker. 47. The method of claim 45, wherein said device is coupled to a fluorimeter or fluorescent microscope. 48. The method of claim 44, wherein said marker is a fluorescent compound. 49. The method of claim 44, wherein said device is comprised of a transparent material. 50. The method of claim 44, further comprising the step of introducing a cellular lysis agent in an inlet port of said device. 51. The method of claim 50, wherein said reagent specifically interacts or detects an intracellular compound. 52. A method of high-throughput, multi-step product formation, the method comprising the steps of: a. introducing a first liquid comprising a precursor to a first inlet port of a microfluidic device; b. introducing a second liquid comprising a reagent, catalyst, reactant, cofactor, or combination thereof to a second inlet port of said microfluidic device, said microfluidic device comprising: i. two or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof, wherein: said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microchannel; at least one conductor element comprised of a symmetric cylinder of a defined radius that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said first liquid and said second liquid are driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing an electric field in said microfluidic channels; at least one conductor element comprised of a symmetric cylinder of a defined radius that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said first liquid and said second liquid are driven across said microfluidic channels so that said first liquid and said second liquid are mixed in said microfluidic channels; and c. collecting said mixed liquid from an outlet port of said device. 53. The method of claim 52, further comprising carrying out iterative introductions of said second liquid, as in (b), to additional inlet ports. 54. The method of claim 52, wherein said reagent is an antibody, a nucleic acid, an enzyme, a substrate, a ligand, a reactant or a combination thereof. 55. A method of analyte detection or assay, comprising the steps of: a. introducing a fluid comprising an analyte to a first inlet port of a microfluidic device, said microfluidic device comprising: i. one or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof wherein: said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microchannel; at least one conductor element comprised of a symmetric cylinder of a defined radius that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said suspension and said reagent are driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing an electric field in said microfluidic channels; an array of conductor elements comprised of symmetric cylinders of a defined radius placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said suspension and said reagent are driven across said microfluidic channels so that said suspension and said reagent are mixed in said microfluidic channels; said microchannels being coated with a reagent for the detection, assay, or combination thereof of said analyte; and detecting, analyzing, or a combination thereof, of said analyte. 56. A microfluidic device comprising one or more inlet ports, one or more outlet ports and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps and one or more micromixers, wherein: said micropumps comprise a passageway for transmitting an electrolyte fluid; a source providing a DC electric field in said microchannel; at least one conductor element comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said at least one conductor element produce electro-osmotic flows so that said electrolyte fluid is driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting an electrolyte fluid; a source providing a DC electric field in said microfluidic channel; at least one conductor element comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said conductor element produce electro-osmotic flows with varied trajectories, and said electrolyte fluid is driven across said microfluidic channels so that said electrolyte fluid is mixed in said microfluidic channels. 57. The microfluidic device of claim 56, wherein said field source is comprised of electrodes of different polarities. 58. The microfluidic device of claim 56, wherein said conductor element is comprised of a conducting strip. 59. The microfluidic device of claim 58, wherein at least one wall of said microfluidic channels comprises said conducting strip. 60. The microfluidic device of claim 56, wherein the shape of said conductor element approximates an arrowhead, teardrop, or ellipse. 61. The microfluidic device of claim 56, wherein said microfluidic channels form a cross-junction, an elbow-junction, a T-junction, a Y-junction, or a combination thereof. 62. The microfluidic device of claim 56, wherein said microfluidic channels are comprised of a transparent material. 63. The microfluidic device of claim 56, wherein said microfluidic channels are comprised of a metal. 64. The microfluidic device of claim 63, wherein said metal is a metal bilayer. 65. The microfluidic device of claim 64, wherein an exposed layer of said bilayer is functionalized to minimize adherence of material conveyed through said device. 66. The microfluidic device of claim 56, wherein said device comprises an away of conductor elements. 67. An apparatus comprising the microfluidic device of claim 56. 68. The microfluidic device of claim 56, wherein said device further comprises a center electrode. 69. A method of cellular analysis comprising the steps of: a. introducing a buffered suspension comprising cells to a first inlet port of a microfluidic device; b. introducing a reagent for cellular analysis to said first inlet or to a second inlet port of said microfluidic device, said microfluidic device comprising: i. one or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof, wherein: a. said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microchannel; at least one conductor element comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said suspension and said reagent are driven across said microfluidic channels; and b. said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microfluidic channels; an anay of conductor elements comprised of asymmetric conductor elements, with either non-uniform surface composition or non-circular cross section placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said suspension and said reagent are driven across said microfluidic channels so that said suspension and said reagent are mixed in said microfluidic channels; and analyzing at least one parameter affected by contact between said suspension and said reagent. 70. The method of claim 69, wherein said reagent is an antibody, a nucleic acid, an enzyme, a substrate, a ligand, or a combination thereof. 71. The method of claim 70, wherein said reagent is coupled to a detectable marker. 72. The method of claim 69, wherein said marker is a fluorescent compound. 73. The method of claim 72, wherein said device is coupled to a fluorimeter or fluorescent microscope. 74. The method of claim 73, wherein said device is comprised of a transparent material. 75. The method of claim 69, further comprising the step of introducing a cellular lysis agent in an inlet port of said device. 76. The method of claim 75, wherein said reagent specifically interacts or detects an intracellular compound. 77. A method of high-throughput, multi-step product formation, the method comprising the steps of: a. introducing a first liquid comprising a precursor to a first inlet port of a microfluidic device; b. introducing a second liquid comprising a reagent, catalyst, reactant, cofactor, or combination thereof to a second inlet port of said microfluidic device, said microfluidic device comprising: i. two or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof, wherein: said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microchannel; at least one conductor element comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said first liquid and said second liquid are driven across said microfluidic channels; and said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microfluidic channels; at least one conductor element comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said first liquid and said second liquid are driven across said microfluidic channels so that said first liquid and said second liquid are mixed in said microfluidic channels; and c. collecting said mixed liquid from an outlet port of said device. 78. The method of claim 77, further comprising carrying out iterative introductions of said second liquid, as in (b), to additional inlet ports. 79. The method of claim 77, wherein said reagent is an antibody, a nucleic acid, an enzyme, a substrate, a ligand, a reactant or a combination thereof. 80. A method of analyte detection or assay, comprising the steps of: a. introducing a fluid comprising an analyte to a first inlet port of a microfluidic device, said microfluidic device comprising: i. one or more inlet ports, at least one outlet port and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps, one or more micromixers, or a combination thereof wherein: a. said micropumps comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microchannel; at least one conductor element comprised of an asymmetric conductor element, with either non-uniform surface composition or non-circular cross section that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said electric field and said at least one conductor element produce electro-osmotic flows so that said suspension and said reagent are driven across said microfluidic channels; and b. said micromixers comprise a passageway for transmitting said suspension and said reagent; a source providing a DC electric field in said microfluidic channels; an anay of conductor elements comprised of asymmetric conductor elements, with either non-uniform surface composition or non-circular cross section placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microfluidic channels, whereby interactions between said electric field and each conductor element produce electro-osmotic flows with varied trajectories, and said suspension and said reagent are driven across said microfluidic channels so that said suspension and said reagent are mixed in said microfluidic channels; c. said microchannels being coated with a reagent for the detection, assay, or combination thereof of said analyte; and detecting, analyzing, or a combination thereof, of said analyte. 81. The microfluidic device of claim 1, wherein said device further comprises a center electrode. 82. The microfluidic device of claim 1, A microfluidic device comprising one or more inlet ports, one or more outlet ports and microfluidic channels in fluid communication with said ports, said channels comprising one or more micropumps and one or more micromixers, wherein: said micropumps comprise a passageway for transmitting an electrolyte fluid: a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microchannel: at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said at least one conductor element produce electro-osmotic flows so that said electrolyte fluid is driven across said microfluidic channels: and said micromixers comprise a passageway for transmitting an electrolyte fluid: a source providing an AC or pulsed AC electric field or pulsed AC electric field with a DC offset in said microfluidic channel: at least one conductor element that is placed in an orientation that is perpendicular to the axis of said electric field, at a location within or proximal to said microchannel, whereby interactions between said field and said conductor element produce electro-osmotic flows with varied trajectories. and said electrolyte fluid is driven across said microfluidic channels so that said electrolyte fluid is mixed in said microfluidic channels wherein said device comprises obstacles in said channels, which impede or change fluid flow in said channels.