CN206557230U - A kind of enzyme linked immunosorbent detection ELISA Plate - Google Patents
A kind of enzyme linked immunosorbent detection ELISA Plate Download PDFInfo
- Publication number
- CN206557230U CN206557230U CN201720250957.0U CN201720250957U CN206557230U CN 206557230 U CN206557230 U CN 206557230U CN 201720250957 U CN201720250957 U CN 201720250957U CN 206557230 U CN206557230 U CN 206557230U
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- plate
- substrate
- neck
- sample
- supporting plate
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Abstract
The utility model discloses a kind of enzyme linked immunosorbent detection ELISA Plate, the utility model includes square supporting plate and square substrate, the middle part of substrate is sample adding cup matrix, supporting plate includes square bottom plate, three sides of bottom plate are provided with neck, substrate is inserted in the neck of bottom plate, the another side of bottom plate is provided with baffle plate, substrate uses transparent material, the plate top surface of supporting plate is provided with the striped that multiple rows of color is differed, the ranking of striped and sample adding cup matrix is corresponded, the Digital ID for identifying sample adding cup rectangular array position is provided with the top surface of a neck parallel with striped.Sample adding cup arranged in matrix of the present utility model is on substrate, positioning mark to sample adding cup is arranged on supporting plate, in sample-adding, substrate and supporting plate are assembled integrally, allow and clearly sample adding cup is positioned in sample-adding, after the completion of sample-adding, separating base plate and supporting plate so that observation of the color fringe of supporting plate without interference with tester to the reagent in sample adding cup.
Description
Technical field
The utility model is related to a kind of enzyme linked immunosorbent detection ELISA Plate.
Background technology
At present in clinical labororatory's detection and biology, immunological investigation, enzyme-linked immunosorbent assay is the most commonly used
A kind of method, it by by antigen or antibody coating on ELISA Plate, in detection serum corresponding antibody or various antigens into
Point, so as to reach the purpose for diagnosing the illness or detecting not clear antigen, in current EUSA, ELISA Plate typically has 96
Hole or 48 orifice plates, sample adding cup are arranged in densely covered matrix, because quantity is more, and technical staff easily sample occurs during sample-adding
Plus wrong position, so that the problem of causing detection mistake.
Utility model content
The technical problems to be solved in the utility model is:A kind of enzyme linked immunosorbent detection ELISA Plate for being easy to be loaded is provided.
In order to solve the above-mentioned technical problem, the utility model includes square supporting plate and square substrate, the middle part of substrate
For sample adding cup matrix, supporting plate includes square bottom plate, and three sides of bottom plate are provided with neck, and substrate is inserted in the neck of bottom plate, bottom
The another side of plate is provided with baffle plate, and one side rotation that a side and the bottom plate of baffle plate do not have neck is connected, and baffle plate is adjacent with two
Neck lateral surface between be provided with locking device, when locking device is in locking state, the neck on baffle plate and bottom plate
Annular is surrounded, substrate is clamped in described annular, is set fluted on the side adjacent with baffle plate on substrate, is rotated in groove
Draw ring is connected with, draw ring has the two states for turning to and being fully located in groove and stretch out groove, and substrate uses transparent material,
The plate top surface of supporting plate is provided with the striped that multiple rows of color is differed, and the ranking of striped and sample adding cup matrix is corresponded, with
The Digital ID for identifying sample adding cup rectangular array position is provided with the top surface of a parallel neck of striped.
For the ease of operating the folding of baffle plate, it is soft that a side of described baffle plate does not have one side of neck to pass through with bottom plate
Plastics are connected, and described locking device includes hook, lock pin and bearing pin, and bearing pin is fixed on baffle plate, and lock pin is fixed on neck,
Hook is rotated with bearing pin and is connected, and links up with the two states during rotation with the lock pin for hanging on lock pin and departing from.
The beneficial effects of the utility model are:Sample adding cup arranged in matrix of the present utility model is on substrate, to sample adding cup
Positioning mark is arranged on supporting plate, and in sample-adding, substrate and supporting plate are assembled integrally so that can be clearly right in sample-adding
Sample adding cup is positioned, after the completion of sample-adding, separating base plate and supporting plate so that the color fringe of supporting plate is without interference with tester to sample adding cup
The observation of interior reagent.
Brief description of the drawings
Fig. 1 is overlooking the structure diagram of the present utility model;
Fig. 2 is left view structural representation of the present utility model;
Fig. 3 is Fig. 2 A partial enlarged drawings;
Fig. 4 is the schematic top plan view of the utility model substrate;
Fig. 5 is the schematic front view of the utility model supporting plate(Broken section);
Fig. 6 is Fig. 5 B partial enlarged drawings;
Fig. 7 is the top view of the utility model supporting plate;
In figure:1st, supporting plate, 2, substrate, 3, locking device, 1-1, striped, 1-2, neck, 1-3, Digital ID, 1-4, gear
Plate, 2-1, sample adding cup matrix, 2-2, groove, 2-3, draw ring, 3-1, lock pin, 3-2, latch hook, 3-3, bearing pin.
Embodiment
A kind of enzyme linked immunosorbent detection ELISA Plate as depicted in figs. 1 and 2, it includes square supporting plate 1 and square substrate
2, as shown in figure 4, the middle part of substrate 2 is sample adding cup matrix 2-1.As shown in fig. 7, supporting plate 1 includes square bottom plate, the three of bottom plate
While being provided with neck 1-2, substrate 2 is inserted in the neck 1-2 of bottom plate, and the another side of bottom plate is provided with baffle plate 1-4, baffle plate 1-4's
One side and bottom plate do not have one side of neck to rotate to be connected, and it is soft that baffle plate 1-4 a side and bottom plate do not have one side of neck to pass through
Matter plastics are connected, it would however also be possible to employ loose-leaf is linked.As shown in figure 3, neck 1-2 adjacent with two baffle plate 1-4 lateral surface it
Between be provided with locking device 3, locking device 3 includes hook 3-2, lock pin 3-1 and bearing pin 3-3, bearing pin 3-3 and is fixed on baffle plate,
Lock pin is fixed on neck, and hook is rotated with bearing pin and is connected, and hook has what is hung on lock pin and depart from during rotation
The two states of lock pin.When locking device 3 is in locking state, baffle plate 1-4 surrounds annular, base with the neck 1-2 on bottom plate
Plate 2 is clamped in described annular, as shown in Figure 5 and Figure 6, sets fluted 2- on substrate 2 on the side adjacent with baffle plate 1-4
Draw ring 2-3 is rotatably connected in 2, groove 2-2, draw ring 2-3, which has to turn to, is fully located in groove 2-2 and stretches out groove 2-2
Two states, substrate 2 uses transparent material, and the plate top surface of supporting plate 1 is provided with the striped 1-2 that multiple rows of color is differed,
Striped 1-2 and sample adding cup matrix 2-1 ranking are corresponded, and are provided with a neck 1-2 parallel with striped 1-1 top surface
Digital ID 1-3 for identifying sample adding cup matrix 2-1 row position.
Application method:Before sample-adding, this ELISA Plate is first maintained at state shown in Fig. 1, according to different colours sum during sample-adding
Word understands technical staff, the position of sample, record sample-adding blueprint.After the completion of sample-adding, locking device 3 is opened, substrate 2 is taken out,
It is easy to observe the change of sample.
Claims (2)
1. a kind of enzyme linked immunosorbent detection ELISA Plate, it is characterised in that:Including square supporting plate and square substrate, the middle part of substrate
For sample adding cup matrix, supporting plate includes square bottom plate, and three sides of bottom plate are provided with neck, and substrate is inserted in the neck of bottom plate, bottom
The another side of plate is provided with baffle plate, and one side rotation that a side and the bottom plate of baffle plate do not have neck is connected, and baffle plate is adjacent with two
Neck lateral surface between be provided with locking device, when locking device is in locking state, the neck on baffle plate and bottom plate
Annular is surrounded, substrate is clamped in described annular, is set fluted on the side adjacent with baffle plate on substrate, is rotated in groove
Draw ring is connected with, draw ring has the two states for turning to and being fully located in groove and stretch out groove, and substrate uses transparent material,
The plate top surface of supporting plate is provided with the striped that multiple rows of color is differed, and the ranking of striped and sample adding cup matrix is corresponded, with
The Digital ID for identifying sample adding cup rectangular array position is provided with the top surface of a parallel neck of striped.
2. enzyme linked immunosorbent detection ELISA Plate according to claim 1, it is characterised in that:One side of described baffle plate and bottom
One side that plate does not have neck is connected by flexible plastic, and described locking device includes hook, lock pin and bearing pin, and bearing pin is fixed on
On baffle plate, lock pin is fixed on neck, hook with bearing pin rotate be connected, hook during rotation with hang on lock pin with
The two states of the lock pin of disengaging.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201720250957.0U CN206557230U (en) | 2017-03-15 | 2017-03-15 | A kind of enzyme linked immunosorbent detection ELISA Plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201720250957.0U CN206557230U (en) | 2017-03-15 | 2017-03-15 | A kind of enzyme linked immunosorbent detection ELISA Plate |
Publications (1)
Publication Number | Publication Date |
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CN206557230U true CN206557230U (en) | 2017-10-13 |
Family
ID=60364139
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CN201720250957.0U Expired - Fee Related CN206557230U (en) | 2017-03-15 | 2017-03-15 | A kind of enzyme linked immunosorbent detection ELISA Plate |
Country Status (1)
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CN (1) | CN206557230U (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108387725A (en) * | 2018-01-13 | 2018-08-10 | 中国医学科学院医学生物学研究所 | A kind of I type of poliovirus, II type, the pre-coated associated detecting method of III type D antigens and its detection kit and application |
-
2017
- 2017-03-15 CN CN201720250957.0U patent/CN206557230U/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108387725A (en) * | 2018-01-13 | 2018-08-10 | 中国医学科学院医学生物学研究所 | A kind of I type of poliovirus, II type, the pre-coated associated detecting method of III type D antigens and its detection kit and application |
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Legal Events
Date | Code | Title | Description |
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GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20171013 Termination date: 20180315 |