Utility model content
For the above-mentioned technical problem in the presence of the prior art, the utility model proposes a kind of automatic immunities
Instrument, the automatic lmunoassays analyzer include:
It is loaded module, is used to sample and reagent being added to lath;
Module is incubated, is used to provide suitable environment temperature for immune response;
The sample-adding module includes the sample-adding local area set gradually along lath moving direction and reagent adding area, and lath can be from
The sample-adding local area is moved to the reagent adding area with straight path;Lath can also be moved to the temperature from the reagent adding area
Module is educated, and the lath can be from the incubation module resets to the reagent adding area.
In one embodiment, the lath is pushed to by the first delivery device from the sample-adding local area with straight path
The reagent adding area.
In one embodiment, first delivery device includes that the first push rod, the first sliding unit and the first driving are single
Member, first push rod can be slided along the first sliding unit, and first push rod can be by lath from the sample-adding local area
The reagent adding area is pushed to straight path, first driving unit is for driving the first sliding unit mobile.
In one embodiment, it is equipped with the first transhipment channel between the sample-adding local area and the reagent adding area, described the
Lath after the completion of being loaded originally is pushed to described add via first transhipment channel from the sample-adding local area by one delivery device
Reagent area.
In one embodiment, the lath is moved to incubation module from the reagent adding area by the second delivery device,
And the lath pushes back to reagent adding area from the incubation module by second delivery device.
In one embodiment, the incubation module includes the first incubation unit and second incubates unit, first temperature
It educates and is provided with the second transhipment channel between unit and the second incubation unit.
In one embodiment, which further includes detection module, is used to carry out sample to be tested
Detection is equipped with third and transports channel, carrying to test sample after the completion of incubating between the incubation module and the detection module
The lath of product is moved to detection module via third transhipment channel.
In one embodiment, the lath for carrying sample to be tested after the completion of the incubation by third delivery device or
Person's mechanical arm is moved to detection module via third transhipment channel.
In one embodiment, it is additionally provided with solid-liquid displacement zone between the second incubation unit and the detection module, examined
The lath for carrying sample to be tested after the completion of survey is completed to be separated by solid-liquid separation in the solid-liquid displacement zone, and completes after being separated by solid-liquid separation
Lath is abandoned in the solid-liquid displacement zone.
In one embodiment, the detection module includes:
Unit is excited, for emitting exciting light;
Reading cell, for receiving the optical signal issued after sample to be tested is excited, and to the received optical signal of institute into
Row acquisition process.
In one embodiment, the excitation unit includes exciter, and the exciter can emit 600~700nm's
Red exciting light, the reading cell include single photon counter, photomultiplier tube, silicon photocell or light-measuring integrating sphere.
In one embodiment, which further includes general liquid loading module, for adding general liquid
It adds on the lath.
In one embodiment, the lath completes the load of general liquid in second transhipment channel.
In one embodiment, which further includes general liquid disk, is contained in the general liquid disk
General liquid.
In one embodiment, which further includes reagent disc, the automatic lmunoassays analyzer structure
It makes as Dual-layer structure, the lower section in the reagent adding area is arranged in the reagent disc, and the general liquid disk is positioned close to institute
State the lower section of general liquid loading module.
In one embodiment, which further includes grillage supplying module, the grillage supplying module
It is described to take grillage mechanism that carry the grillages of blank plates from described including taking grillage mechanism, storehouse and the 4th delivery device
It is taken out in storehouse, the 4th delivery device is used to the blank plates taken out from the storehouse pushing to sample-adding local area.
In one embodiment, which further includes pre-dilution module, and the pre-dilution module is used for
Pre-dilution processing is carried out to the solution comprising sample to be tested.
Compared with prior art, the utility model has the prominent advantages that, full-automatic immune point disclosed by the utility model
Analyzer has abandoned rotary-disk type structure when adding sample to be tested and reagent, is transported lath from sample-adding mechanism using straight path
To reagent adding mechanism, the preparation process for the completion sample to be tested being simple and efficient reduces manufacturing cost, simplifies installation, reduces
Failure rate.Further, since lath can move back and forth between reagent adding mechanism and incubation module, so that this is practical new
Immunity analysis instrument described in type more automatically realizes three the steps even purpose of multi-step incubation.
Other features and advantages of the utility model will illustrate in the following description, also, partial from specification
In become apparent, or understood and implementing the utility model.The purpose of this utility model and other advantages can pass through
Specifically noted structure is achieved and obtained in the specification, claims and drawings.
Specific embodiment
The embodiments of the present invention is described in detail below with reference to accompanying drawings and embodiments, whereby to the utility model
How applied technology method solves technical problem, and the realization process for reaching technical effect can fully understand and implement.
If it should be noted that do not constitute conflict, each feature in each embodiment and each embodiment in the utility model
It can be combined with each other, be formed by technical solution and both be within the protection scope of the present invention.
Fig. 1 provides a kind of automatic lmunoassays analyzer according to the present utility model, as shown in Figure 1 comprising sample-adding mould
Block and incubation module 2.Sample-adding module is used to sample and reagent being added to blank plates.It incubates module 2 and is used to be lath
The sample and reagent of upper carrying occur chemiluminescence immunoassay reaction and provide suitable environment temperature.
Wherein, sample-adding module includes the sample-adding local area 11 set gradually along lath moving direction and reagent adding area 12, lath
Reagent adding area 12 can be moved to from sample-adding local area 11 with straight path.Lath can also be moved to incubation mould from reagent adding area 12
Block 2, and reagent adding area 12 can be reset to from module 2 is incubated.
In the present invention, the sample includes but is not limited to sample to be tested and the solution comprising sample to be tested.Reagent
Including but not limited to dilution, cleaning solution, general liquid, reaction reagent or solvent etc..
The temperature that can usually use is incubated as 43 DEG C, 37 DEG C, room temperature or 4 DEG C, 37 DEG C are common temperature in laboratory
Educate the optimal reactive temperature of temperature and the combination of most of antigen-antibodies.In most cases, antigen-antibody reaction is generally at 37 DEG C
After 1-2 hours, the product of generation is up to peak.To accelerate reaction, reaction can be improved in a certain range in experimentation
Temperature and during the reaction continuous oscillation come increase antigen-antibody contact probability.
The automatic lmunoassays analyzer has abandoned rotary-disk type structure when preparing sample to be tested, using straight path by lath
It is transported to reagent adding mechanism from sample-adding mechanism, the preparation process for the completion sample to be tested being simple and efficient reduces manufacturing cost,
Installation is simplified, failure rate is reduced.Further, since lath can move back and forth between reagent adding mechanism and incubation module,
So that three step of the realization even purpose of multi-step incubation that the analyzer more automates.
In one embodiment, as shown in Fig. 2, lath passes through the first delivery device 4 from sample-adding local area 11 with straight path
Push to reagent adding area 12.There is first delivery device 4, so that lath is directly moved to from sample-adding local area 11 with linear distance
Reagent adding area 12 avoids when preparing sample to be tested using rotary-disk type structure in the past, and analyzer has to specific until turntable
Region could be loaded when rotating to predeterminated position and reagent adding.
In one embodiment, as shown in figure 3, the first delivery device 4 includes the first push rod 41, the first sliding unit and the
One driving unit, the first push rod 41 can be slided along the first sliding unit, and can push lath from sample-adding local area 11 with straight line
Track pushes to reagent adding area 12, and the first driving unit is for driving the first sliding unit mobile.Specifically, the first sliding unit
Including the first sliding block 42 and the first sliding rail 43, the first sliding block 42 is connect by the first synchronous belt 44 with first motor 45, and first is sliding
Block 42 can be slided along the first sliding rail 43.First sliding block 42, which is able to drive the promotion lath of push rod 41 and is moved to from sample-adding local area 11, to be added
Reagent area 12.
In one embodiment, as depicted in figs. 1 and 2, it is loaded between local area 11 and reagent adding area 12 and is equipped with the first transhipment
Channel 13, the first delivery device 4 push to the lath after the completion of being loaded originally from sample-adding local area 11 via the first transhipment channel 13
Reagent adding area 12.
In one embodiment, lath is moved to from reagent adding area 12 by the second delivery device and incubates module 2, and is passed through
Second delivery device pushes back to reagent adding area 12 from module 2 is incubated.The structure of second delivery device can be with the first delivery device
Structure it is identical, the lath after incubation need to return reagent adding area 12 add additive reagent when, as long as control the second delivery device
In motor reversal.The structure of second delivery device can be identical as the structure of the first delivery device, can also be under
The structure for stating the 4th delivery device is identical.
In one embodiment, as shown in Figure 1, incubating module 2 includes that the first incubation unit 21 and second incubate unit 22.
In one embodiment, as shown in Figure 1, being provided with second between the first incubation unit 21 and the second incubation unit 22
Transport channel 23.
In one embodiment, as shown in Figure 1, the automatic lmunoassays analyzer further includes detection module 3, for treating test sample
Product are detected.
In one embodiment, channel 24 is transported as shown in Figure 1, incubating and being equipped with third between module 2 and detection module 3,
The lath for carrying sample to be tested after the completion of incubation is moved to detection module 3 via third transhipment channel 24.
In one embodiment, the lath for carrying sample to be tested after the completion of incubating is by third delivery device via the
Three transhipment channels 24 are moved to detection module 3, it can also be transported channel via third by mechanical arm and be moved to detection
Module.The structure of the third delivery device can be identical as the structure of the first delivery device, can also be with following 4th pushers
The structure of structure is identical.
In one embodiment, solid-liquid displacement zone 25 is additionally provided between the second incubation unit 22 and detection module 3.If no
Rereading is needed, then after the completion of reading, the lath for carrying sample to be tested is completed to be separated by solid-liquid separation in solid-liquid displacement zone 25, and
The lath after being separated by solid-liquid separation will be completed to abandon in solid-liquid displacement zone 25.If there is rereading, then will complete to read for the first time
Lath after number is retracted along former track after third transhipment channel 24 removes and is again introduced into the progress rereading of detection module 3.
In one embodiment, as shown in figure 4, detection module 3 includes excitation unit 31 and reading cell 32.Excite unit 31
For emitting exciting light.Reading cell 32 is used to receive the optical signal issued after sample to be tested is excited, and received to institute
Optical signal is acquired processing.In the case of this kind, automatic lmunoassays analyzer disclosed by the utility model is full-automatic light activation
Learn luminometer.It should be understood that automatic lmunoassays analyzer disclosed by the utility model is also possible to full-automatic magnetic particle
Chemiluminescence detector or other Full-automatic chemiluminescence analyzers.
Light-induced chemiluminescent method is one of common method of chemiluminescence analytical technique, can be used for immunoassay detection, faces
It is mainly used for the detection of disease on bed.It is combined in a certain range by photosensitive particulate and luminous particle, generates ion-oxygen energy
The transmitting of amount issues optical signal, to detect to sample to be tested.Wherein, Photoactive compounds are filled with inside photosensitive particulate,
And luminophor and lanthanide series are filled with inside luminous particle.It is photosensitive under the excitation of red laser (600~700nm)
Particle releases the singlet oxygen ion (4 μ S) of upper state, and propagation distance is about 200nm.When photosensitive particulate and luminous particle
Distance it is close enough when, the singlet oxygen ion of photosensitive particulate release can reach luminous particle, and pass through a series of chemistry
Reaction, launches the light of 520~620nm high level, and is detected by instrument.In this reaction system, the concentration of particle is very low,
Collision probability is smaller, and background signal is faint.Only after photosensitive particulate and luminous particle are combined by immune response, can just it send out
Apparent light is projected, therefore the sensitivity of system is very high.In medical diagnosis on disease, common detection pattern includes three to four groups
Point:The luminous particle of envelope antigen or antibody, the antigen of biotin or digoxigenin labeled or antibody, Avidin or anti-digoxin packet
The photosensitive particulate of quilt neutralizes antigen or antibody etc..The above each component passes through the above incubation reaction of two steps and determined antigen or antibody
In conjunction with, and sample to be tested is qualitatively or quantitatively detected by the power of chemiluminescence amount.With traditional ELISA
Method is compared, it has the characteristics that homogeneous, high sensitivity and easy to operate is easy to automate.Therefore, application prospect is very wide
It is wealthy.
In this embodiment, excitation unit 31 includes exciter, and exciter can emit the red excitation of 600~700nm
Light;Reading cell 32 includes single photon counter, photomultiplier tube, silicon photocell or light-measuring integrating sphere.
In a preferred embodiment, as shown in figure 5, excitation unit 31 is other than including exciter, it further include exciting light
Switch 311, excitation light switch 311 are used to control the conducting and blocking of the exciting light emitted by excitation unit.
In one embodiment, as shown in figure 5, excitation light switch 311 includes rotating part 3111, on the side wall of rotating part 3111
There are two through-hole 3112, two through-holes 3112 to pass through the axle center of rotating part 3111 for tool.When the line of two through-holes 3112 is vertical,
Excitation light switch 311 is in the open state, excites light conduction, and exciting light can be irradiated to by through-hole 3112 to be located under opening 34
On the sample to be tested of side.When the line of two through-holes 3112 is non-vertical, excitation light switch 311 is in close state, exciting light
It is blocked, exciting light can not be irradiated on the sample to be tested for being located at 34 lower section of opening.
In a preferred embodiment, reading cell 32 includes receiving photoswitch 321, receives photoswitch 321 for controlling
The conducting or blocking of sample to be tested generated optical signal after being excited.
In one embodiment, as shown in fig. 6, receiving photoswitch 321 includes baffle 3211 and crank and rocker mechanism, baffle
3211 lower part is equipped with the first circular hole 3212;The lower part of crank and rocker mechanism is equipped with the second circular hole 3213, crank and rocker mechanism
Movement enables the first circular hole 3212 and the second circular hole 3213 to overlap, when 3213 phase of the first circular hole 3212 and the second circular hole
It when being mutually overlapped, receives photoswitch 321 and opens, when the first circular hole 3212 and the second circular hole 3213 are not overlapped, receive photoswitch
321 close.
In this embodiment, crank and rocker mechanism includes the first rotation section 3214 and the second rotation section 3215, the first rotation
Portion 3214 is fixed on baffle 3211;Second rotation section 3215 is rotatablely connected the first rotation section 3214, the second circular hole 3213
The lower part of second rotation section 3215 is set.First rotation section 3214 rotates under the drive of the drive, and drives second turn
Dynamic portion 3215 rotates, so that when the second circular hole 3213 turns to the position of corresponding first circular hole 3212, the first circular hole
3212 and second circular hole 3213 overlap.
In one embodiment, as shown in figure 4, excitation light switch 311 and reception photoswitch 321 are all connected with control device 331,
Control device 331 receives photoswitch 321 and closes, and work as and receive photoswitch 321 for making when excitation light switch 311 is connected
When conducting, excitation light switch 311 is closed.Preferably, control device 331 is driver, and one end of the driver connects exciting light
Switch 311, other end connection receives photoswitch 321, when connection, needs so that rotary driver in any case, excitation light switch 311
It all can not be in the open state simultaneously with photoswitch 321 is received.
In one embodiment, as shown in figure 4, the detection module 3 further includes optical path component 33, optical path component includes along reception
Half-reflecting half mirror 332, lens 333 and the optical filter 334 that the direction of light is set gradually, half-reflecting half mirror 332 are arranged in exciting light
Channel and the intersection for receiving optical channel.Half-reflecting half mirror 332 can not only be ended non-targeted by the exciting light of target wavelength
The exciting light of wavelength, while the luminous signal of target wavelength caused by sample to be tested can be reflected.Preferably, half-reflecting half mirror
With the intersection of 45 degree of overturning angle setting exciting lights and reception light.Through half-reflecting half mirror 332 reflect as produced by sample to be tested
Optical signal enter reading cell 32 by lens.
In a preferred embodiment, as shown in Figure 1, full-automatic light-induced chemiluminescent detector further includes that general liquid adds
Module is carried, for general liquid to be added to lath.Preferably, general liquid loading module is equipped with independent third sample arm (figure
In be not shown).Under normal conditions, lath from first incubation unit 21 be moved to the second incubation unit 22 during, second
It transports in channel 23 and general liquid is added by third sample arm.
In a preferred embodiment, as shown in Figure 1, automatic lmunoassays analyzer further includes reagent disc 10, reagent disc
Reagent to be added is held in 10.
In one embodiment, as shown in fig. 7, the upper end opening of reagent disc 10 is configured to circle.Reagent disc 10 includes spacious
Mouth device 101 and the rotary part 102 that the bottom of open device 101 is set and open device 101 is driven to rotate, open device
Scanner section 103 is provided on 101 side wall, scanning means can identify the category of open 101 interior reagent of device by scanner section 103
Property.Scanner section 103 is the through-hole for being provided with open 101 side of device, and the reagent inside open device 101 is arranged in test chamber
In 104, the label on test chamber 104 can be revealed by through-hole.Wherein, test chamber 104 can be reagent bottle, examination
Pipe, beaker or flask etc..Scanner section 103 is flushed with the height of the label on test chamber 104, can facilitate scanning means, example
Such as card reader or scanner, the label on test chamber 104 is scanned, so as to avoid the identification of operator's manual scanning
The step of, reduce the risk of error.Scanning means is by the test chamber of the current location scanned (i.e. at reagent suction port)
Information be sent in controller, controller is judged, whether the reagent in the test chamber of current location is required examination
Agent, if so, reagent arm acts;If it is not, then rotary part is driven to be rotated, go to the test chamber of the next position currently
Position simultaneously repeats the above process, therefore by above-mentioned automatically scanning function, is able to maintain the consistency of result.Rotary part band
Dynamic opening device 101 and its internal test chamber 104 rotate together with, and so that test chamber 104 is reached reagent suction port, to try
Agent arm draws reagent from test chamber.The reagent disc is by opening up scanner section on the side wall of open device, whenever reagent position
In current location, scanning means can identify that attribute of current location reagent, such as the type of reagent etc. are believed by scanner section
Breath, therefore the step of reagent is taken out simultaneously manual scanning by operator in conventional method from open device is omitted, it can drop
The risk of low error, and guarantee the consistency of reagent.
In this embodiment, as shown in Figure 1, automatic lmunoassays analyzer further includes general liquid disk 20, in general liquid disk 20
It is contained with general liquid.General liquid can be the solution including photosensitive microballoon.Third mechanical arm draws general liquid out of general liquid disk,
And it adds it on the lath in the second transhipment channel.
In this embodiment, as shown in Figure 1, automatic lmunoassays analyzer is configured to Dual-layer structure, 10 He of reagent disc
The general setting of liquid disk 20 is loaded local area 11, reagent adding area 12, incubation module 2 and detection module 3 and is arranged on upper layer in lower layer.Tool
Body, the lower section in reagent adding area 12 is arranged in reagent disc 10, and general liquid disk 20 is positioned close to the lower section of general liquid loading module.
This kind of Dual-layer design, can shorten size together, so that the even closer smoothness of the cooperation between each component, thus further
Improve detection efficiency.
In a preferred embodiment, as shown in Figure 1, automatic lmunoassays analyzer further includes grillage supplying module 5.It should
Grillage supplying module 5 is for providing blank plates.
In one embodiment, as shown in figure 8, grillage supplying module 5 includes that grillage mechanism 51, storehouse 52 and the 4th is taken to push away
Mechanism 50 is sent, takes grillage mechanism 51 to take out the grillage for carrying blank plates from storehouse 52, the 4th delivery device 50 is used for
The blank plates taken out from storehouse 52 are pushed into sample-adding local area 11.Grillage 53 successively overlays in storehouse 52, takes when above-mentioned
As soon as grillage mechanism 51 often takes out laminate frame 53 from the top of storehouse 52, then grillage transmission mechanism drives storehouse 52 to rise a position
Set namely an adjacent grillage 53 between height.Successively the grillage 53 of a file is taken in this way, then one file of artificial threading
Grillage 53.
Grillage mechanism 51 is taken to include the second sliding block (positioned at the lower section of grillage 53, being not shown in the figure) and the second optical axis 511, the
Two sliding blocks are connect by the second synchronous belt 512 with the second motor (not shown), and the second sliding block can be along the second optical axis 511
Sliding, the both ends of the second optical axis 511 pass through the second fixed block 513 and are fixed on bottom plate 514.The upper surface of second sliding block is equipped with
Handgrip, handgrip can take out grillage 53 from storehouse 52, and move under the drive of the second sliding block.
4th delivery device 50 includes the 4th push rod 501, the 4th sliding unit and the 4th driving unit, the 4th push rod 501
It can be slided along the 4th sliding unit, and blank plates can be pushed to be moved to sample-adding local area 11, the 4th driving unit is for driving
Dynamic 4th sliding unit is mobile.4th sliding unit includes Four-slider 502 and the 4th optical axis 503, and Four-slider 502 passes through the
Four synchronous belts 504 are connect with the 4th motor 506, and Four-slider 502 can be slided along the 4th optical axis 503, the 4th optical axis 503
Both ends pass through the 4th fixed block 505 and are fixed in pusher arms 507.
4th delivery device 50 is completed on the blank plates push-in sample-adding local area 11 on grillage 53 when a lath pushes
Afterwards, the 5th sliding block 111 drives the width between the mobile adjacent slat of lath clamping device 112 on sample-adding local area 11, together
When, the first sliding block drives grillage 53 to move equally the width between an adjacent slat, so that push rod 501 can push down
On one lath to sample-adding local area 11.
In a preferred embodiment, pre- dilute as shown in Figure 1, automatic lmunoassays analyzer further includes pre-dilution module 6
Module 6 is released for carrying out pre-dilution processing to the solution comprising sample to be tested.Preferably, pre-dilution module 6 includes pre-dilution plate
(not shown) and oscillator (not shown) control sample arm when the solution comprising sample to be tested needs pre-dilution
The solution is added in the pre-dilution plate in pre-dilution module 6, oscillator is then controlled and oscillation treatment is carried out to pre-dilution plate,
With the solution comprising sample to be tested after being diluted.
In the automatic lmunoassays analyzer shown in above-mentioned, the main flow of detection includes:
1) grillage mechanism 51 is taken to take out the grillage 53 for carrying blank plates from storehouse 52;
2) blank plates are pushed into sample-adding local area 11 by the 4th delivery device 50 from storehouse 53, complete sample in sample-adding local area 11
This addition;
3) lath for having added sample to be tested is pushed to reagent adding area 12 from sample-adding local area 11 by the first delivery device 4,
The addition of the completion of reagent adding area 12 reagent;
4) the second delivery device will add after reagent lath and push to the first incubation unit 21 from reagent adding area 12, and
First, which incubates unit 21, completes first step incubation;
5) lath for carrying sample to be tested after incubating the first step is moved to the second incubation from the first incubation unit 21
Unit 22 carries out second step incubation, in moving process, when carrying the lath of sample to be tested by the second transhipment channel, adds
Add general liquid.
6) third delivery device pushes the lath for carrying sample to be tested after the completion of incubation from the second incubation unit 22
To detection module 3, read in detection module 3.
If needing to add additive reagent in the lath for carrying sample to be tested after completing first step incubation, then passing through
The lath for carrying sample to be tested is retracted into reagent adding area 12 and adds additive reagent by the second delivery device, has added additive reagent
Afterwards, 4) -6 are repeated the above process).
In one embodiment, as shown in figure 9, sample-adding module further includes the first sample arm 14 and the second sample arm 15,
In, the first sample arm 14 is for adding the solution comprising sample to be tested, and the second sample arm 15 is for adding reaction reagent.First adds
Needle pond (not shown) can be washed by first after the completion sample-adding movement of sample arm 14 to be cleaned, the second sample arm 15 plus reaction examination
Needle pond (not shown) can be washed by second after the completion of agent to be cleaned.Therefore in this embodiment, 14 He of the first sample arm
Second sample arm 15 can carry out sample-adding to lath simultaneously and originally operate with reagent adding, avoid and had in turntable structure until turning
Lath on disk can just be added the solution comprising sample to be tested or addition reaction reagent operation after rotating to designated position,
So as to shorten detection time.
It in this embodiment, further include sample carrier 7, the sample carrier 7 is for carrying sample to be detected.
In one embodiment, it as shown in figure 9, the blank plates taken out from storehouse 52 push to sample-adding local area 11, holds
The lath for being loaded with the solution comprising sample to be tested pushes to reagent adding area 12 from sample-adding local area 11 and carries mixed solution
Lath pushes to the first incubation unit 21 from reagent adding area 12 and is completed by same delivery device, which is denoted as the 5th and pushes away
Mechanism 30 is sent, structure can be identical as the first delivery device 4, can also be identical as the 4th delivery device 50.
It should be understood that above-mentioned push step can also be realized by three independent delivery devices respectively, although independent
Three kinds of delivery devices can increase the flexibility that detector transports lath, but this kind setting will increase the complexity of mechanical structure
Property, cause detector volume to increase, while manufacturing cost increases.
In this embodiment, it is moved to the second incubation unit 22 from the first incubation unit 21 via the second transhipment channel 23,
And be moved to detection module 3 via third transhipment channel 24 from the second incubation unit 22 and also completed by same delivery device, it should
Delivery device is denoted as the 6th delivery device 40, and structure can be identical as the first delivery device 4, can also be with the 4th delivery device
50 is identical.
Above description is merely a prefered embodiment of the utility model, but scope of protection of the utility model is not limited to
This, any those skilled in the art can be easy to carry out and be altered or varied in technical scope disclosed by the utility model, and
This be altered or varied should be covered within the scope of the utility model.Therefore, the protection scope of the utility model is answered
Subject to the scope of protection of the claims.