Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of microchannel array plate, device for acquiring liquid drops by the same and liquid drop generation method

A micro-channel plate and micro-channel technology, applied in chemical instruments and methods, transportation and packaging, fluid controllers, etc., can solve problems such as poor experimental parallelism, low success rate, and difficulty in achieving high-throughput production.

Active Publication Date: 2016-11-09
因纽美瑞克斯公司
View PDF5 Cites 16 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

These shortcomings make it difficult for the microfluidic devices commonly found in bioanalytical chemistry laboratories to be more widely used.
In response to the above problems, cn104741158A proposed a device and method for generating micro-droplets by using inertial force, but in this device, a capillary array is used as a droplet forming device, and the capillary array needs to be drawn, the success rate is low, and the thickness of the capillary is uneven , prone to clogging, poor experimental parallelism, and difficult to achieve high-throughput production

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of microchannel array plate, device for acquiring liquid drops by the same and liquid drop generation method
  • Preparation method of microchannel array plate, device for acquiring liquid drops by the same and liquid drop generation method
  • Preparation method of microchannel array plate, device for acquiring liquid drops by the same and liquid drop generation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0103] The cooperation of embodiment 1 microchannel plate and collection device

[0104] Microchannel plate with 1.5mL centrifuge tube

[0105] Add 1ml of the second liquid into the centrifuge tube. Because the second liquid is easy to generate air bubbles, it must be added slowly. After the air bubbles are formed, you can use a 1ml pipette to replace the tip with a new pipette, and quickly aim at the air bubbles to pump out the air. The air bubbles will disappear immediately. was blown apart.

[0106] Assembly diagram as Figure 4 shown. 1 bolt, 1.1 bolt head, 1.2 bolt lower surface, 1.3 male thread, 1.4 through hole, 2 spacer, 3 microchannel array plate, 4 connection part, 4.1 connection part head, 4.2 connection part lower end surface, 4.3 female thread, 4.4 Inner end, 5 1.5mL centrifuge tubes (the caps are omitted here). After the two threads are tightened, fix the microchannel plate and place it lightly in the centrifuge tube filled with the second liquid.

[0107] M...

Embodiment 2

[0111] The droplets produced by the device of the present invention are used in digital chain reaction (dPCR) detection of trace DNA samples based on TaqMan probes

[0112] The second liquid formulation in this example was isopropyl laurate / Abilem 180 v / v 83 / 17 solution and the collection device was a 1.5 ml centrifuge tube.

[0113] The preparation method of the first liquid

[0114] First prepare the following mixture (1), wherein the primers are designed based on a 223bp sequence in lambda phage DNA for PCR amplification, and TaqMan probes are also designed based on this sequence.

[0115]

[0116]After obtaining the mixed solution (1), take 99 μl of the mixed solution and add 1 μl of DNA template. This DNA template is the product after agarose gel purification, and its concentration is determined by Nanodrop. Add 1 μl of 1.00*10^6 copy and 1 μl of 1.00*10^5 to 99 μl of the mixture (1) respectively to obtain reaction samples A and B. in

[0117]

A

B

...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a preparation method of a microchannel array plate. The method comprises the steps of: (1) taking two different optical fiber glass rods, wherein one cannot be corroded by corrosive liquid and one can be corroded by corrosive liquid, arranging the two glass rods closely, and melting the two glass rods under high temperature into a whole, drawing the whole one time or multiple times into a long and slender glass rod, cutting the fine drawn glass rod into small sheets to obtain a microchannel plate blank; (2) corroding the blank to remove the core so as to obtain a through-hole equipped microchannel plate; and (3) conducting hydrophobic treatment on the microchannel plate. The microchannel array plate and collection device provided by the invention can cooperate with an acceleration generation device to achieve high throughput and rapid production of uniform micron-scale liquid drops by inertia force.

Description

technical field [0001] The invention relates to a preparation method of a microchannel array plate, a device for obtaining liquid droplets and a method for producing liquid droplets. Background technique [0002] Emulsion droplet technology is a crucial part of many molecular biology experiments. Uniform, stable, and compatible liquid droplets for biological experiments have been demonstrated in many technologies and applications. Among them, technologies and methods such as cell culture, sample separation, digital polymerase chain reaction and emulsion whole genome amplification are common. Droplet technology is likely to become the technical cornerstone of next-generation sequencing, third-generation PCR reactions, and related high-throughput biological tests. On the one hand, many isolated and independent solution environments caused by droplets can form many tiny reaction vessels, which greatly reduces the amount of samples; Excellent choice for molecular amplificatio...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): B01L3/00
CPCB01L3/0241B01L2200/12B01L2200/061B01L2300/0861B01L2300/0829B01L2400/0409B01L2300/165B01L2200/0673B01L2300/0832B01L2300/161B01F23/4145B01F23/41B01F25/20B01F35/71725
Inventor 黄岩谊陈子天廖珮宇张芳丽
Owner 因纽美瑞克斯公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products