Abstract: A method for removing fluid in a microfluidic device, the microfluidic device having a fluid channel, a first well, and a second well, the first well and the second well being coupled to a first end of the fluid channel, the method including applying a pressure difference between the second well and the first well, and applying a pressure difference between the first end and a second end of the fluid channel being below a certain threshold, for at least partly removing a first fluid from a first supply line coupled between the first well and the first end of the fluid channel.

Abstract: A microfluidic assembly (1;57) has at least one microfluidic flow path (17,27,29,35,38;82,85,95) and at least one inlet port (11,13,15;81,97,101) coupled to the flow path (17,27,29,35,38;82,85,95). The microfluidic assembly (1;57) has a first microfluidic device (7;63) that executes a microfluidic process and has a second microfluidic device (9;61). The microfluidic assembly (1;57) has an interface (5;65). The interface (5;65) couples the first microfluidic device (7;63) and the second microfluidic device (9;61).

Abstract: A medium is provided, being adapted to be applied in electrophoretic separation of nucleic acids. The medium comprises a staining reagent adapted to stain nucleic acids. Said medium further comprises a urea derivative, adapted to interact with said staining reagent and thereby providing an enhanced staining of said nucleic acids. Further, an electrophoresis device is provided, adapted to perform electrophoretic separation of nucleic acids, comprising the before medium and comprising electrodes for applying an electrical field across the medium. A method to perform electrophoresis using the before electrophoresis device and medium is provided.

Abstract: A method for handling samples in a microfluidic system is described. The microfluidic system includes an injection channel fluidically coupled to an injection point adapted for injecting an amount of fluid, a first sample well containing a first sample, the first sample well being fluidically coupled with the injection channel, and a second sample well containing a second sample, the second sample well being fluidically coupled with the injection channel. The method includes moving the second sample from the second sample well towards the first sample well.

Abstract: A fluid supply unit is described, with the fluid supply unit comprising a fluid dispenser with an orifice adapted for dispensing a fluid, and a microfluidic device comprising an inlet port located at one of the faces of the microfluidic device. The fluid supply unit is adapted for establishing a fluidic contact between a droplet formed at the fluid dispenser's orifice and an inlet port of the microfluidic device, and the fluid supply unit is adapted for electrophoretically moving charged compounds from the droplet towards the inlet port.

Abstract: A medium is provided, being adapted to be applied in electrophoretic separation of nucleic acids. The medium comprises a staining reagent adapted to stain nucleic acids. Said medium further comprises a urea derivative, adapted to interact with said staining reagent and thereby providing an enhanced staining of said nucleic acids. Further, an electrophoresis device is provided, adapted to perform electrophoretic separation of nucleic acids, comprising the before medium and comprising electrodes for applying an electrical field across the medium. A method to perform electrophoresis using the before electrophoresis device and medium is provided.

Abstract: A method for handling samples in a microfluidic system is described. The microfluidic system includes an injection channel fluidically coupled to an injection point adapted for injecting an amount of fluid, a first sample well containing a first sample, the first sample well being fluidically coupled with the injection channel, and a second sample well containing a second sample, the second sample well being fluidically coupled with the injection channel. The method includes moving the second sample from the second sample well towards the first sample well.

Abstract: US 2004/0119070A1 (D1) discloses an integrated microchip design, wherein glass microchips can be linearly moved against one another, in order to connect or disconnect capillary channels in the microchips. In contrast thereto, the invention provides a plastic material microfluidic device having an interface for coupling and flow controlling a flow path between the plastic and a second microfluidic device, which can be made e.g. of glass. This allows coupling e.g. different material microfluidic devices e.g. in order to make use of advantages of different material type microfluidic devices.

Abstract: A microfluidic system comprises a first reservoir, an injection channel fluidically coupled to the first reservoir and to an injection point adapted for injecting an amount of fluid, and a side channel fluidically coupled to the injection channel at an intersection point located between the first reservoir and the injection point, the side channel being fluidically coupled with a second reservoir. Both the injection channel and the side channel are at least partly filled with a first substance and the second reservoir is at least partly filled with a second substance. The first substance is a gel and the second substance is a buffer solution. The side channel's cross section is larger than the injection channel's cross section.