CN217202691U

CN217202691U - Micro-fluidic chip for insect symbiotic fungus single cell isolated culture

Info

Publication number: CN217202691U
Application number: CN202122878200.5U
Authority: CN
Inventors: 帅梦溪; 赖城玲; 庞琨; 陈强; 俞晓平
Original assignee: China Jiliang University
Current assignee: China Jiliang University
Priority date: 2021-11-23
Filing date: 2021-11-23
Publication date: 2022-08-16
Anticipated expiration: 2031-11-23

Abstract

The invention discloses a micro-fluidic chip for isolated culture of insect symbiotic fungi unicells, which relates to the technical field of micro-fluidic chips and is divided into three layers of structures from top to bottom, wherein the three layers of structures comprise a first PDMS plate, a second PDMS film and a third PDMS plate in sequence, the first PDMS plate is provided with a total sample inlet, a total sample outlet, a microcavity outlet and a culture solution channel loaded with microchambers, and each microcavity comprises a straight microcavity main channel, a semicircular microcavity side channel and a microcavity sample outlet channel; an outer gas valve set for switching on and off a sample outlet channel of the microcavity and an inner gas valve set for switching on and off a side channel of the microcavity are arranged on the third PDMS plate; the invention provides a micro-fluidic chip for single cell separation culture of insect symbiotic fungi, which integrates the functions of single cell screening, culture, separation, temperature-variable regulation, convenience for comparison experiments and the like, can realize the single cell culture of the insect symbiotic fungi, is rapid and convenient in process, and can be regulated and controlled in real time.

Description

Micro-fluidic chip for insect symbiotic fungus single cell separation culture

Technical Field

The invention relates to the technical field of microfluidic chips, in particular to application to the unicellular isolation culture of insect symbiotic fungi.

Background

A large number of symbiotic fungi exist in insect bodies, and the symbiotic fungi not only have various types, but also play an important role in the life activities of the insect such as growth, development, reproduction, nutritional metabolism, resistance variation, immune function and the like. The definite identification of insect symbiotic bacteria and the functions thereof is the key for researching the symbiotic relationship between the symbiotic bacteria and the insects. However, due to technical limitations and the characteristic of easy pollution of the insect symbiotic fungi in vitro culture, a great deal of manpower and technical cost are required for research.

Microfluidics is a technology for precisely controlling and manipulating microscale fluids, particularly submicron structures, and is also called lab-on-a-chip or microfluidic chip technology. The basic operation units of sample preparation, reaction, separation, detection and the like in the processes of biological, chemical and medical analysis are integrated on a micron-scale chip, and the whole analysis process is automatically completed. Due to its great potential in the fields of biology, chemistry, medicine and the like, the method has been developed into a new research field crossing the disciplines of biology, chemistry, medicine, fluid, electronics, materials, machinery and the like. Due to the micron-scale structure, the fluid exhibits and develops specific properties in the microfluidic chip that are different from the macro-scale, thus developing unique analytical properties. Meanwhile, the device has the advantages of light volume, small amount of used samples and reagents, low energy consumption, high reaction speed, capability of massively parallel processing, disposability and the like.

Most of the micro-fluidic chips on the market and the micro-fluidic chip devices applied for patent are suitable for detection, no device special for culturing insect symbiotic fungi is provided, and the controllable variables in culture are few, so that the requirements of experiments are difficult to meet.

Disclosure of Invention

Aiming at the defects of the existing products and technologies, the invention provides the micro-fluidic chip for the single cell isolation and culture of insect symbiotic fungi, which integrates the functions of single cell screening, culture, isolation, variable temperature regulation, convenience for comparison experiments and the like, can realize the single cell culture of the insect symbiotic fungi, and has the advantages of rapid and convenient process and real-time regulation.

In order to solve the technical problems, the invention is realized by the following technical scheme:

a micro-fluidic chip for the isolation culture of insect symbiotic fungi single cells is divided into three layers of structures from top to bottom, namely a first layer PDMS plate, a second layer PDMS membrane and a third layer PDMS plate in sequence, wherein the first layer PDMS plate and the third layer PDMS plate are polydimethylsiloxane PDMS plates, the second layer PDMS membrane is a polydimethylsiloxane PDMS thin film, and the adjacent two layers of structures are bonded up and down and are overlapped at edges to form a sealed state;

the first layer PDMS plate is provided with a total sample inlet, a total sample outlet, a plurality of micro-chamber sample outlets and a plurality of culture solution channels loaded with micro-chambers, one end of each culture solution channel is connected with the total sample inlet, the other end of each culture solution channel is connected with the total sample outlet, and each culture solution channel is provided with a plurality of micro-chambers connected in series; each micro-cavity chamber comprises a straight micro-cavity chamber main channel, a semicircular micro-cavity chamber side channel and a micro-cavity chamber sample outlet channel, wherein two ends of each side channel are connected with the corresponding main channel, a capturing cavity and an intercepting channel are sequentially arranged on the main channel from a liquid inlet side to a liquid outlet side, the capturing channel, the capturing cavity and the intercepting channel are all positioned between two connecting positions of the side channels and the main channel, the inner diameter of the intercepting channel is smaller than that of the capturing channel, one end of the micro-cavity chamber sample outlet channel is connected with the capturing cavity, and the other end of the micro-cavity chamber sample outlet channel is connected with a micro-cavity chamber sample outlet; the main channels of two adjacent micro-chambers on each culture solution channel are sequentially connected in series, the other end of the main channel of the head micro-chamber is connected with a total sample inlet, and the other end of the main channel of the tail micro-chamber is connected with a total sample outlet;

the third layer of PDMS plate is provided with a plurality of external gas valve groups for switching on and off the micro-cavity sample outlet channels, the external gas valve groups correspond to the culture solution channels one by one, the external gas valve groups can switch on and off all the micro-cavity sample outlet channels on the corresponding culture solution channels, when the external gas valve groups are ventilated, the second layer of PDMS membrane is inflated and expanded by the external gas valve groups to extrude the micro-cavity sample outlet channels in the first layer of PDMS plate, and the micro-cavity sample outlet channels on the corresponding first layer of PDMS plate are cut off; when the outer gas valve group is not ventilated, a micro-cavity sample outlet channel corresponding to the first layer of PDMS plate is opened, an outer gas valve group gas inlet and an outer gas valve group gas outlet for the gas in the outer gas valve group to enter and exit are arranged on the third layer of PDMS plate, and a gas inlet connecting hole corresponding to the position of the outer gas valve group gas inlet and a gas outlet connecting hole corresponding to the position of the outer gas valve group gas outlet are arranged on the first layer of PDMS plate and the second layer of PDMS film;

the third layer of PDMS plate is provided with a plurality of internal air valve groups for switching on and off the side channels of the micro-chamber, the internal air valve groups correspond to the culture solution channels one by one, the internal air valve groups can switch on and off all the side channels of the micro-chamber on the corresponding culture solution channels, when the internal air valve groups are ventilated, the second layer of PDMS membrane is inflated by the internal air valve groups to expand and extrude the side channels of the micro-chamber in the first layer of PDMS plate, and the side channels of the micro-chamber on the corresponding first layer of PDMS plate are cut off; when the inner valve bank is not ventilated, a side channel of the micro-chamber corresponding to the first layer of PDMS plate is opened, an inner valve bank air inlet and an inner valve bank air outlet for air in the inner valve bank to enter and exit are arranged on the third layer of PDMS plate, and air inlet connecting holes corresponding to the air inlet of the inner valve bank and air outlet connecting holes corresponding to the air outlet of the inner valve bank are arranged on the first layer of PDMS plate and the second layer of PDMS membrane.

Preferably, the culture solution channel on the first layer of PDMS slab is a pore channel etched on the surface of the PDMS slab by using photolithography technique.

Preferably, the culture solution channel is a microfluidic channel which is 100-1000um long and 5-50um in diameter and leads to the total sample outlet from a position below the total sample inlet.

Preferably, the number of the culture solution channels is 2.

Preferably, the micro-chamber sample outlet channel is a micro-flow pore channel with the diameter of 5-50um and leading from the micro-chamber to the position below the micro-chamber sample outlet.

Preferably, the micro-chamber is a groove sunk into the first layer of PDMS slab.

Preferably, the number of the micro-chambers is 10.

Preferably, in the micro chamber, the diameter of the main channel is 5-50 um; the diameter of the side channel is 5-50 um; the diameter of the capture channel is 2-25 um; the diameter of the capture cavity is 5-50 um; the diameter of the interception channel is 2-5 um.

Preferably, the diameters of the total sample inlet, the micro-cavity sample outlet, the total sample outlet, the outer gas valve bank gas inlet, the inner gas valve bank gas inlet, the outer gas valve bank gas outlet and the inner gas valve bank gas outlet are all matched with the diameter of the middle part of the 100 microliter pipetting gun head.

Under normal conditions, the difference between the flow resistance of the main channel and the flow resistance of the side channel is not large, when cells which are small in the channels are captured in the capturing channel, the main channel is blocked, the flow resistance is increased, and the solution flows out of the side channel to the next capturing area to be sequentially captured, so that the function of single cell separation is realized. The single cells are isolated in the micro-chamber and the culture can be continued.

The chip of the invention can overcome the difficulties of difficult separation, easy pollution, difficult culture condition exploration, low flux and the like of insect symbiotic fungi, realizes single cell level separation, high flux culture and cell extraction of the insect symbiotic fungi, has convenient and rapid operation, high separation efficiency, large flux, less energy consumption and recycling.

Drawings

FIG. 1 is a schematic diagram of a chip layer structure according to the present invention.

FIG. 2 is a schematic view of a micro-chamber according to the present invention.

1-a first layer of PDMS plate, 2-a second layer of PDMS film, 3-a third layer of PDMS plate, 4-a total sample inlet, 5-a micro chamber sample outlet, 6-a culture solution channel, 7-a total sample outlet, 8-an outer gas valve set gas inlet, 9-an inner gas valve set gas inlet, 10-an outer gas valve set, 11-an outer gas valve set gas outlet, 12-an inner gas valve set gas outlet, 13-an inner gas valve set, 14-a micro chamber main channel, 15-a micro chamber side channel, 16-a micro chamber capture channel, 17-a micro chamber sample outlet channel, 18-a capture cavity, 19-a micro chamber interception channel and A-a micro chamber.

Detailed Description

The invention is further described with reference to the accompanying drawings and the embodiments.

As shown in figure 1, the micro-fluidic chip for the isolation culture of the insect symbiotic fungi single cell is divided into three layers of structures from top to bottom, wherein the three layers of structures are a first layer PDMS plate 1, a second layer PDMS membrane 2 and a third layer PDMS plate 3, the first layer PDMS plate 1 and the third layer PDMS plate 3 are polydimethylsiloxane PDMS plates, the second layer PDMS membrane 2 is a polydimethylsiloxane PDMS thin film, and the adjacent two layers of structures are bonded up and down and the edges of the adjacent two layers of structures are overlapped to form a sealed state.

The first layer PDMS plate 1 is provided with 1 total sample inlet 4, 1

total sample outlet

7, 10

micro-chamber sample outlets

5 and 2 culture solution channels 6 loaded with micro-chambers A, one end of each of the 2 culture solution channels is connected with the total sample inlet 4, and the other end of each of the 2 culture solution channels is connected with the total sample outlet 7; the culture solution channel on the first layer PDMS plate 1 is a pore canal carved on the surface of the PDMS plate by adopting a photoetching technology, the channel is a microfluidic pore canal which is 100-1000um long and 5-50um in diameter and leads to the total sample outlet 7 from the position below the total sample inlet 4, the number of the microfluidic pore canals is 2, and the number of the microfluidic pore canals can be increased or decreased according to actual needs.

Each culture solution channel is provided with 5 serially connected micro-chambers A, and the number of the micro-chambers A can be increased or decreased according to actual needs. Each micro-chamber A comprises 1 straight micro-chamber main channel 14, 1 semicircular micro-chamber side channel 15 and 1 micro-chamber sample outlet channel 17, and two ends of each side channel 15 are connected with the corresponding main channel 14; the main channels 14 of two adjacent micro chambers A on each culture solution channel 6 are sequentially connected in series, the other end of the main channel 14 of the head micro chamber A is connected with the total sample inlet 4, the other end of the main channel 14 of the tail micro chamber A is connected with the total sample outlet 7, a capturing channel 16, a capturing cavity 18 and an intercepting channel 19 are sequentially arranged on the main channel 14 from the liquid inlet side to the liquid outlet side, the capturing channel 16, the capturing cavity 18 and the intercepting channel 19 are all located between two joints of the side channel 15 and the main channel 14, and the inner diameter of the intercepting channel 19 is smaller than the inner diameter of the capturing channel 16.

In the micro-chamber A, the diameter of the main channel 14 is 5-50 um; the diameter of the side channel 15 is 5-50 um; the diameter of the capture channel 16 is 2-25 um; the capture chamber 18 is 5-50um in diameter; the diameter of the interception channel 19 is 2-5 um.

One end of the microcavity sample outlet channel 17 is connected with the capture cavity 18, the other end of the microcavity sample outlet channel is connected with the microcavity sample outlet 5, the diameter of the microcavity sample outlet channel 17 is 5-50um, and the microcavity sample outlet channel A leads to a micro-flow pore channel at the position below the microcavity sample outlet 5.

The third layer PDMS plate 3 is provided with 1 group of outer gas valve groups 10 which are formed by combining 2 gas valves and are used for switching on and off micro-chamber sample outlet channels 17, the outer gas valve groups 10 correspond to the culture solution channels 6 one by one, the outer gas valve groups 10 can be switched on and off and correspond to all the micro-chamber sample outlet channels 17 on the culture solution channels 6, when the outer gas valve groups 10 are ventilated, the second layer PDMS membrane 2 is inflated and expanded by the outer gas valve groups 10 to extrude the micro-chamber sample outlet channels 17 in the first layer PDMS plate 1, and the micro-chamber sample outlet channels 17 corresponding to the first layer PDMS plate 1 are cut off; when not ventilating in the outer valves 10, correspond microcavity outlet channel 17 on the first layer PDMS board 1 and open, be equipped with outer valves air inlet 8 and outer valves gas outlet 11 that supplies the interior gas business turn over of outer valves on the third layer PDMS board 3, all be equipped with the connecting hole of admitting air that corresponds with outer valves air inlet 8 position and the connecting hole of giving vent to anger that corresponds with outer valves gas outlet 11 position on first layer PDMS board 1 and the second floor PDMS membrane 2.

The third layer of PDMS plate 3 is provided with 1 group of internal air valve sets 13 which are formed by combining 2 air valves and are used for switching on and off the microcavity chamber side channels 15, the internal air valve sets 13 correspond to the culture solution channels 6 one by one, the internal air valve sets 13 can switch on and off all the microcavity chamber side channels 15 on the corresponding culture solution channels 6, when the internal air valve sets 13 are internally ventilated, the second layer of PDMS membrane 2 is inflated and expanded by the internal air valve sets 13 to extrude the microcavity chamber side channels 15 in the first layer of PDMS plate 1, and the microcavity chamber side channels 15 on the corresponding first layer of PDMS plate 1 are cut off; when the inner valve set 13 is not ventilated, the side channel 15 of the micro chamber corresponding to the first layer of PDMS plate 1 is opened, the third layer of PDMS plate 3 is provided with an inner valve set air inlet 9 and an inner valve set air outlet 12 for air in and out of the inner valve set, and the first layer of PDMS plate 1 and the second layer of PDMS membrane 2 are both provided with an air inlet connecting hole corresponding to the position of the inner valve set air inlet 9 and an air outlet connecting hole corresponding to the position of the inner valve set air outlet 12.

The diameters of the total sample inlet 4, the micro-cavity sample outlet 5, the total sample outlet 7, the outer gas valve group gas inlet 8, the inner gas valve group gas inlet 9, the outer gas valve group gas outlet 11 and the inner gas valve group gas outlet 12 are all matched with the diameter of the middle part of a pipetting gun head of 100 microliters.

The culture cavity is a groove sunk into the first PDMS plate, the bottom of the whole chip is provided with a set of self-testing constant-temperature amplification thermal module, the temperature control precision is within 1 degree, the temperature range is 32-98 degrees, the time control range is 1-180 hours, and the culture cavity has the functions of starting reminding and ending reminding.

The chip is manufactured by adopting a photoetching process, and a photoetching machine, a glue homogenizing instrument, an oven and other instruments are used during manufacturing. The manufacturing material is mainly PDMS glue.

The first stage of high-flux accurate sorting: opening the outer gas valve group 10, namely closing the micro-cavity sample outlet 5 and the sample outlet channel 17 connected with the micro-cavity; at the same time, the internal air valve set 13 is closed, i.e. the microcavity chamber side channel 15 is opened. Adding culture solution containing target strains into the chip through the total sample inlet 4 for separation and screening, wherein under the normal condition, the flow resistance difference between the main channel 14 and the side channel 15 of the micro-chamber is not large, when cells which are small in the channels are captured by the capture channel 16 and sent into the capture cavity 18, then the cells are intercepted in the capture cavity 18 by the interception channel 19, at the moment, the main channel is blocked, the flow resistance is increased, the solution flows out to the next micro-chamber A from the side channel, the cells of the target strains can be sequentially separated and screened, and redundant culture solution and non-target strains finally flow out from the total sample outlet 7.

Second-stage target cell extraction: stopping sampling, and closing the outer gas valve group 10, namely opening the micro-cavity sample outlet 5 and the micro-cavity sample outlet channel 17; and simultaneously, the internal air valve set 13 is opened, namely, the microcavity chamber side channel 15 is closed. The pressure difference is brought by the pressure closing of the side channel 15, and pure culture solution without any strain is introduced during the pressure closing, so that the separated target strain cells in the capture cavity 18 enter the sample outlet channel 17 of the micro-chamber, and the target strain cells are separated and extracted.

The invention provides a micro-fluidic chip for separating and unicellular culturing insect symbiotic fungi, which integrates the functions of cell screening, culturing, separating, variable temperature regulation and control, convenience for comparison experiments and the like, can realize unicellular culturing of the insect symbiotic fungi, has quick and convenient process and can realize real-time regulation and control. The chip mainly designs a separation channel according to various parameters of target bacteria, carries out high-flux rapid screening in a short time, and cultures the screened target bacteria in a stable environment, so that some bacteria which cannot be technically cultured in vitro can be cultured in a single cell mode under the condition of leaving a parasitic host, and can be taken out for identification after the culture is finished. The invention does not depend on other instruments and equipment, and has the advantages of high running speed, high efficiency, strong specificity and simple and convenient operation.

It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the inventive concept, which falls within the scope of the present invention. Therefore, the protection scope of the present patent should be subject to the appended claims.

Claims

1. A micro-fluidic chip for insect symbiotic fungus single cell isolation culture is characterized in that: the structure comprises three layers of structures from top to bottom, namely a first layer PDMS plate (1), a second layer PDMS film (2) and a third layer PDMS plate (3) in sequence, wherein the first layer PDMS plate (1) and the third layer PDMS plate (3) are polydimethylsiloxane PDMS plates, the second layer PDMS film (2) is a polydimethylsiloxane PDMS film, and the adjacent two layers of structures are bonded up and down and the edges of the adjacent two layers of structures are overlapped to form a sealed state;

the first layer PDMS plate (1) is provided with a total sample inlet (4), a total sample outlet (7), a plurality of microcavity sample outlets (5) and a plurality of culture solution channels (6) loaded with microchambers (A), one ends of the culture solution channels (6) are connected with the total sample inlet (4), the other ends of the culture solution channels are connected with the total sample outlet (7), and each culture solution channel (6) is provided with a plurality of serially connected microchambers (A); each micro chamber (A) comprises a straight micro chamber main channel (14), a semicircular micro chamber side channel (15) and a micro chamber sample outlet channel (17), two ends of each side channel (15) are connected with the corresponding main channel (14), a capture channel (16), a capture cavity (18) and an interception channel (19) are sequentially arranged on each main channel (14) from a liquid inlet side to a liquid outlet side, each capture channel (16), each capture cavity (18) and each interception channel (19) are positioned between two connecting positions of the side channels (15) and the corresponding main channel (14), the inner diameter of each interception channel (19) is smaller than the inner diameter of each capture channel (16), one end of each micro chamber sample outlet channel (17) is connected with the corresponding capture cavity (18), and the other end of each micro chamber sample outlet channel (5) is connected with one micro chamber sample outlet; the main channels (14) of two adjacent micro chambers (A) on each culture solution channel (6) are sequentially connected in series, the other end of the main channel (14) of the head micro chamber (A) is connected with the total sample inlet (4), and the other end of the main channel (14) of the tail micro chamber (A) is connected with the total sample outlet (7);

the third-layer PDMS plate (3) is provided with a plurality of outer air valve groups (10) for switching on and off micro-cavity sample outlet channels (17), the outer air valve groups (10) correspond to the culture solution channels (6) one by one, the outer air valve groups (10) can switch on and off all the micro-cavity sample outlet channels (17) on the corresponding culture solution channels (6), when the outer air valve groups (10) are ventilated, the second-layer PDMS membrane (2) is inflated and expanded by the outer air valve groups (10) to extrude the micro-cavity sample outlet channels (17) in the first-layer PDMS plate (1), and the micro-cavity sample outlet channels (17) on the corresponding first-layer PDMS plate (1) are cut off; when the outer valve bank (10) is not ventilated, a micro-chamber sample outlet channel (17) corresponding to the first layer of PDMS plate (1) is opened, an outer valve bank air inlet (8) and an outer valve bank air outlet (11) for the air in the outer valve bank (10) to enter and exit are arranged on the third layer of PDMS plate (3), and an air inlet connecting hole corresponding to the position of the outer valve bank air inlet (8) and an air outlet connecting hole corresponding to the position of the outer valve bank air outlet (11) are arranged on the first layer of PDMS plate (1) and the second layer of PDMS membrane (2);

a plurality of inner air valve groups (13) for opening and closing microcavity chamber side channels (15) are arranged on the third layer PDMS plate (3), the inner air valve groups (13) correspond to the culture solution channels (6) one by one, the inner air valve groups (13) can open and close all microcavity chamber side channels (15) on the corresponding culture solution channels (6), when the inner air valve groups (13) are ventilated, the second layer PDMS membrane (2) is inflated and expanded by the inner air valve groups (13) to extrude the microcavity chamber side channels (15) in the first layer PDMS plate (1), and the microcavity chamber side channels (15) on the corresponding first layer PDMS plate (1) are cut off; when not ventilating in interior valves (13), correspond microcavity side passageway (15) on the first layer PDMS board (1) and open, be equipped with interior valves air inlet (9) and interior valves gas outlet (12) that supply interior valves (13) interior gas to go into and out on third layer PDMS board (3), all be equipped with on first layer PDMS board (1) and second layer PDMS membrane (2) with interior valves air inlet (9) position correspond the inlet connection hole and with the outlet connection hole that interior valves gas outlet (12) position corresponds of air inlet (9).

2. The microfluidic chip for the isolated culture of the insect symbiotic fungi unicell of claim 1, wherein the culture solution channel (6) on the first layer of PDMS plate (1) is a pore channel lithographically depicted on the surface of PDMS plate.

3. The microfluidic chip for the single cell isolation and culture of insect symbiotic fungi according to claim 2, wherein the culture solution channel (6) is a microfluidic channel which is 100-1000um long and 5-50um in diameter and leads to the total sample outlet (7) from a position below the total sample inlet (4).

4. The microfluidic chip for the unicell isolation and culture of insect symbiotic fungi according to claim 2, wherein the number of the culture solution channels (6) is 2.

5. The microfluidic chip for the isolated culture of the single cells of the insect symbiotic fungi according to claim 1, wherein the micro-chamber sample outlet channel (17) is a micro-flow channel which has a diameter of 5-50um and leads from the micro-chamber (A) to a position below the micro-chamber sample outlet (5).

6. The microfluidic chip for the unicell isolation culture of insect symbiotic fungi according to claim 1, wherein the micro chamber (a) is a groove sunk into the first layer of PDMS slab (1).

7. The microfluidic chip for the unicell separation culture of insect symbiotic fungi according to claim 6, wherein the number of the micro-chambers (A) is 10.

8. The microfluidic chip for the unicell separation culture of insect symbiotic fungi according to claim 6, wherein in the micro chamber (A), the diameter of the main channel (14) is 5-50 um; the diameter of the side channel (15) is 5-50 um; the diameter of the capture channel (16) is 2-25 um; the diameter of the capture cavity (18) is 5-50 um; the diameter of the interception channel (19) is 2-5 um.

9. The micro-fluidic chip for the unicell isolation culture of the insect symbiotic fungi according to claim 1, wherein the diameters of the total sample inlet (4), the microcavity sample outlet (5), the total sample outlet (7), the outer gas valve group gas inlet (8), the inner gas valve group gas inlet (9), the outer gas valve group gas outlet (11) and the inner gas valve group gas outlet (12) are all matched with the diameter of the middle part of a pipetting gun head of 100 microliters.