摘要:
Provided is a linker functional group patterning method for biomolecule immobilization. The patterning method includes preparing a coating composition including a hydrophobic group-containing silane compound and a hydrophilic group-containing silane compound; forming a surface tension control layer by coating the coating composition on a substrate for biomoleucle immobilization; and forming a linker functional group pattern on the surface tension control layer using a coating composition including a linker functional group-containing compound followed by thermal treatment. The linker functional group pattern is formed in a uniform size and distribution and contains high-density linker functional groups.
摘要:
A multi-channel fluorescence measuring optical system and a multi-channel fluorescence sample analyzer using the optical system are provided. The multi-channel fluorescence measuring optical system, which irradiates light onto a plurality of sample channels and detecting fluorescence radiated from samples (m), includes: a light source (10); an integrator (20) for giving the light irradiated from the light source a uniform intensity distribution; a sample holder (30) having a plurality of sample channels on which the samples (m) are mounted, wherein the samples (m) are exited by the light emitted from the integrator (20); a beam splitter (25) between the integrator (20) and the sample holder (30) for dividing the incident light in a predetermined ratio; and a light detecting unit (40) for detecting fluorescence from the samples (m) through the beam splitter (25). Preferably, the light intensities of fluorescence images are detected using optical fiber bundles and photodiodes, the manufacturing cost can be greatly reduced, and the optical system can be miniaturized.
摘要:
A multi-channel fluorescence measuring optical system and a multi-channel fluorescence sample analyzer using the optical system are provided. The multi-channel fluorescence measuring optical system, which irradiates light onto a plurality of sample channels and detecting fluorescence radiated from samples, includes: a light source (60a-d); an integrator (70) for giving the light irradiated from the light source a uniform intensity distribution; a sample holder (80) having a plurality of sample channels on which the samples (m) are mounted, wherein the samples are exited by the light emitted from the integrator; and a beam splitter (75) between the integrator and the sample holder for dividing the incident light in a predetermined ratio. Since the light intensities of fluorescence images are detected using optical fiber bundles (85a-d) and photodiodes (89a-d), the manufacturing cost can be greatly reduced, and the optical system can be miniaturized.
摘要:
Provided is a device (100) for printing a droplet onto a substrate (30). The device includes (100): a droplet generating member that is needle-shaped (20) and comprises a receiving portion that is disposed vertically and receives a solution (22), and a discharge hole (23) connected to the receiving portion and formed on the bottom of the receiving portion so that the solution can be discharged from the receiving portion; a substrate (30) that is disposed below the droplet generating member, and includes a target portion to which the droplet discharged (10a) from the discharge hole (23) of the droplet generating member (20) is dropped and attached; a voltage applier (50) applying a voltage to the droplet (10a) so that the droplet can be dropped onto the target portion of the substrate; a volume measuring unit measuring the volume of the droplet; and a droplet control unit maintaining the volume of the droplet at a predetermined level based on the measured volume of the droplet (60,62,63,64,66).
摘要:
Provided is a method of reducing the temperature difference between a pair of substrates (103, 121), which are a high-temperature substrate (103) and a low-temperature substrate (121), including a heat transfer facilitating layer (110) which has a higher thermal conductivity than air and can hold particles (150) between those substrates (103, 121), and maintaining close contacts among the high-temperature substrate (103), the heat transfer facilitating layer (110), and the low-temperature substrate (121) so that the formation of an air layer can be prevented both between the high-temperature substrate (103) and the heat transfer facilitating layer (110), and between the low-temperature substrate (121) and the heat transfer facilitating layer (110). In addition, provided is a fluid reaction device (100) comprising: a microfluidic reaction chip (120) that accommodates a fluid (F); a heater (101) that heats the microfluidic reaction chip (120); and a heat transfer facilitating layer (110) that is interposed between the microfluidic reaction chip (120) and the heater (101), has a higher thermal conductivity than air and can hold particles (150), wherein the heater (101), the heat transfer facilitating layer (110), and the microfluidic reaction chip (120) are fixed to one another so that the formation of an air layer can be prevented both between the heater (101) and the heat transfer facilitating layer (110), and between the microfluidic reaction chip (120) and the heat transfer facilitating layer (110).
摘要:
Provided is an apparatus for printing a biomolecular droplet onto a substrate (30, 70) using an electric charge concentration effect, the apparatus including: an electric field forming electrode (20) that is needle-shaped, is made of a conductive material, is disposed vertically, and includes an accommodating area (22) in which the biomolecular droplet including micro magnetic beads is accommodated and a nozzle (23) formed on a bottom end of the accommodating area (22) through which the biomolecular droplet is discharged; a substrate (30, 70) that is disposed below the electric field forming electrode (20), includes a target surface (31, 72) onto which the biomolecular droplet discharged from the nozzle (23) of the electric field forming electrode (20) is deposited, and is grounded; a magnet (40) that is disposed below the substrate (30, 70) to attract the micro magnetic beads by a magnetic force towards the substrate (30, 70); and an open circuit type voltage applying unit (60) which is electrically connected to the electric field forming electrode (20) to apply a charge to the electric field forming electrode (20), and causes the biomolecular droplet to be ejected onto the target surface (31, 72) of the substrate (30, 70) due to the force generated by the charge in the electric field forming electrode (20) and a charge induced by the charge in the electric field forming electrode (20) in the substrate (30, 70).
摘要:
An ultra small fluorescence detector capable of detecting in real time reaction undergoing in a micro chamber having a predetermined volume and disposed on a microfluid chip is provided. The fluorescence detector for detecting in real time PCR amplification undergoing in the microfluid chip having a micro chamber with a predetermined volume includes a light source generating an excitation beam, a first optical system capable of irradiating the excitation beam having a predetermined spot size to the micro chamber, a first detector, and a second optical system reflecting a fluorescent beam derived from the excitation beam having the predetermined spot size in the micro chamber to the first detector. Accordingly, the fluorescence detector is designed such that light emitted by a light source is focused between a first mirror and an objective lens. Therefore, the spot size of an excitation beam transmitted by the objective lens is largely formed so that the excitation beam can be irradiated on the whole micro chamber of the microfluid chip, thereby detecting a fluorescent beam on a broader area.
摘要:
An apparatus for focusing a particle in a sheath flow, the apparatus comprising: a sheath fluid inlet for injecting a sheath fluid; a first flow channel for conveying a fluid, wherein the first flow channel extends from the sheath fluid inlet to the fluid outlet and is formed such that a channel extending from the sheath fluid inlet is divided into two subchannels that extend further and are then merged into one channel; and a second flow channel that extends from the sample fluid inlet to the sample fluid outlet, wherein the second flow channel is in fluid communication with the first flow channel at the merged channel region through the sample fluid outlet so as to introduce a particle in a sample into a sheath fluid conveyed through the first flow channel.