Virus detection elisa plate

Abstract

The utility model discloses a virus detection elisa plate and relates to the field of elisa plates. The virus detection elisa plate comprises an elisa plate main body, a reagent bottle plate is movably inserted into the elisa plate main body, a control mechanism is arranged outside the elisa plate main body, the control mechanism comprises a fixing plate which is movably arranged outside the elisa plate main body, the fixing plate is movably clamped outside the reagent bottle plate, and the reagent bottle plate is movably clamped outside the fixing plate. The fixing plate is used for fixing the position of the reagent bottle plate, the pushing plate is movably arranged in the elisa plate main body, the pushing plate is arranged on the lower surface of the reagent bottle plate, and the pushing plate is used for pushing the reagent bottle plate upwards. According to the virus detection elisa plate, the two sides of the reagent bottle plate are fixed by arranging the fixing plate, and meanwhile, the fixing plate and the clamping plate are moved away at the later stage, so that fixation of the reagent bottle plate and the pushing plate is relieved, the pushing plate is pushed to quickly and stably move out of the reagent bottle plate, and the use stability and convenience of the elisa plate are improved.

Description

Technical Field

[0001] This utility model relates to the field of enzyme-linked immunosorbent assay (ELISA) plate technology, specifically to an ELISA plate for virus detection. Background Technology

[0002] A virus detection ELISA plate is a specially designed microplate typically used in enzyme-linked immunosorbent assays (ELISA) to detect viral antigens or antibodies. During virus detection, antigens, antibodies, and other biomolecules adsorb onto the surface of the ELISA plate and react with the viral antigens or antibodies in the sample being tested, thus enabling the detection of the virus.

[0003] The existing ELISA plates have the problem that the reagent bottle can easily detach from the plate when it is handled externally, and if it is well fixed, the reagent bottle will be difficult to remove.

[0004] The reason for this problem is that during the use of ELISA plates, reagent vials need to be inserted into the plate. Before use, the ELISA plate is moved. If the movement is too fast or the plate is flipped, the reagent vials may fall out of the plate. Since the reagent vials are specially treated before use, and most of them are connected in a row, if the sides of the vials are too tightly connected to the plate, it will be difficult to remove them later. If they are pushed from below, the force between the vials will be uneven, causing the connection points between the vials to bend. Therefore, we propose a virus detection ELISA plate. Utility Model Content

[0005] In order to overcome the shortcomings of the existing technology, this utility model proposes a virus detection enzyme label plate, which solves the problem that the reagent bottle of the existing enzyme label plate is easy to detach from the inside of the enzyme label plate when it is handled from the outside, and if it is well fixed, it will be difficult to remove the reagent bottle.

[0006] To solve the above-mentioned technical problems, the basic technical solution proposed by this utility model is as follows: a virus detection ELISA plate, comprising an ELISA plate body, a reagent bottle plate being movably inserted into the interior of the ELISA plate body, and a control mechanism being provided on the exterior of the ELISA plate body. The control mechanism includes a fixing plate, which is movably disposed on the exterior of the ELISA plate body. The fixing plate is movably engaged with the exterior of the reagent bottle plate. The fixing plate is used to fix the position of the reagent bottle plate. A pushing plate is movably disposed inside the ELISA plate body. The pushing plate is disposed on the lower surface of the reagent bottle plate and is used to push the reagent bottle plate upward.

[0007] Preferably, a connecting plate is fixedly connected to the lower surface of the fixing plate, and the outside of the connecting plate abuts against the outside of the enzyme-labeled plate body.

[0008] Preferably, a snap-fit ​​plate is fixedly connected to the outside of the connecting plate, a snap-fit ​​groove is provided on the outside of the enzyme labeling plate body, the push plate is slidably connected inside the snap-fit ​​groove, the snap-fit ​​plate is movably inserted into the inside of the snap-fit ​​groove, and the snap-fit ​​plate is movably snapped onto the outside of the push plate.

[0009] Preferably, a snap-fit ​​block is fixedly connected to the outside of the reagent bottle plate, and a glue plate is fixedly connected to the outside of the enzyme labeling plate body. The snap-fit ​​block is movably snapped into the inside of the glue plate, and the fixing plate is slidably connected to the upper surface of the glue plate and the snap-fit ​​block.

[0010] Preferably, a limiting rod is fixedly connected inside the main body of the enzyme-labeled plate, a sliding block is movably sleeved on the outside of the limiting rod, a connecting rod is fixedly connected to the outside of the sliding block, the connecting rod is movably inserted into the inside of the main body of the enzyme-labeled plate, and the end of the connecting rod is fixedly connected to the outside of the connecting plate.

[0011] Preferably, a spring is movably sleeved on the outside of the limiting rod, the spring being fixedly connected to the outside of the sliding block and the inside of the enzyme-labeled plate body.

[0012] The beneficial effects of this utility model are:

[0013] The technical solution of this utility model involves moving the fixing plates to both sides, causing the sliding block to compress the internal spring of the ELISA plate body. Then, the reagent bottle is placed inside the ELISA plate body, and the fixing plates are released. The springs then generate tension, pushing the sliding block to move. The fixing plates move to a position above the adhesive plate and the locking block, at which point the locking plates will be fitted onto both ends of the push plate. To remove the reagent bottle later, the fixing plates and locking plates need to be moved, and then the push plate is pushed upwards to remove a set of reagent bottles. By setting the fixing plates to secure the reagent bottle on both sides, and simultaneously removing the fixing plates and locking plates later, the fixation of the reagent bottle and push plate is released, allowing the push plate to quickly and stably remove the reagent bottle, increasing the stability and convenience of using the ELISA plate. Attached Figure Description

[0014] To more clearly illustrate the technical solutions in the embodiments of this utility model or the prior art, the drawings used in the description of the embodiments or the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this utility model. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0015] Figure 1 This is a schematic diagram of the overall structure of this utility model;

[0016] Figure 2 This is an exploded view of the main body of the enzyme-labeled plate of this utility model;

[0017] Figure 3 This is an exploded view of the external exterior of the push plate of this utility model;

[0018] Figure 4 This is an exploded view of the interior of the enzyme-labeled plate of this utility model.

[0019] In the diagram: 1. Main body of the ELISA plate; 101. Reagent bottle plate; 102. Glue plate; 103. Snap-fit ​​block; 2. Fixing plate; 201. Snap-fit ​​plate; 202. Push plate; 203. Connecting plate; 204. Spring; 205. Limiting rod; 206. Connecting rod; 207. Snap-fit ​​groove; 208. Sliding block. Detailed Implementation

[0020] To make the objectives, technical solutions, and advantages of the embodiments of this utility model clearer, the technical solutions in the embodiments of this utility model are described clearly and completely. Obviously, the described embodiments are only some embodiments of this utility model, not all embodiments. Based on the embodiments of this utility model, all other embodiments obtained by those skilled in the art without creative effort are within the protection scope of this utility model.

[0021] This application provides a virus detection ELISA plate, which solves the problem that existing ELISA plates have reagent bottles that are easy to detach from the plate during handling, and that if they are well secured, the reagent bottles are difficult to remove.

[0022] To better understand the above technical solutions, the following will provide a detailed explanation of the technical solutions in conjunction with the accompanying drawings and specific implementation methods.

[0023] This utility model discloses a binding device for organizing archives.

[0024] According to the appendix Figure 1-4 As shown, the system includes an ELISA plate body 1, a reagent vial 101 is movably inserted into the ELISA plate body 1, and a control mechanism is provided on the outside of the ELISA plate body 1. The control mechanism includes a fixing plate 2, which is movably disposed on the outside of the ELISA plate body 1 and is movably snapped onto the outside of the reagent vial 101. The fixing plate 2 is used to fix the position of the reagent vial 101. A pushing plate 202 is movably disposed inside the ELISA plate body 1 and is disposed on the lower surface of the reagent vial 101. The pushing plate 202 is used to push the reagent vial 101 upward.

[0025] A connecting plate 203 is fixedly connected to the lower surface of the fixing plate 2. The outside of the connecting plate 203 abuts against the outside of the enzyme labeling plate body 1. A snap-fit ​​plate 201 is fixedly connected to the outside of the connecting plate 203. A snap-fit ​​groove 207 is opened on the outside of the enzyme labeling plate body 1. A push plate 202 is slidably connected to the inside of the snap-fit ​​groove 207. The snap-fit ​​plate 201 is movably inserted into the inside of the snap-fit ​​groove 207. The snap-fit ​​plate 201 is movably snapped onto the outside of the push plate 202. A snap-fit ​​block 103 is fixedly connected to the outside of the reagent bottle plate 101. A gel plate 102 is fixedly connected to the outside of the enzyme labeling plate body 1. The snap-fit ​​block 103 is movably snapped onto the inside of the gel plate 102. The fixing plate 2 is slidably connected to the upper surface of the gel plate 102 and the snap-fit ​​block 103.

[0026] An ELISA plate body 1 is internally fixedly connected to a limiting rod 205. A sliding block 208 is movably sleeved on the outside of the limiting rod 205. A connecting rod 206 is fixedly connected to the outside of the sliding block 208. The connecting rod 206 is movably inserted into the inside of the ELISA plate body 1. The end of the connecting rod 206 is fixedly connected to the outside of the connecting plate 203. A spring 204 is movably sleeved on the outside of the limiting rod 205. The spring 204 is fixedly connected to the outside of the sliding block 208 and is fixedly connected to the inside of the ELISA plate body 1.

[0027] By moving the fixing plate 2 to both sides, the fixing plate 2 causes the connecting plate 203 to move. At this time, the connecting plate 203 also causes the connecting rod 206 to move. The connecting rod 206, in turn, causes the sliding block 208 to move. The sliding block 208 then slides outside the limiting rod 205. During its movement, the sliding block 208 will press against the internal compression spring 204 of the ELISA plate body 1. After the fixing plate 2 slides away from the position above the gel plate 102, the reagent bottle 101 is placed inside the ELISA plate body 1. At this time, the locking block 103 will be actively engaged inside the gel plate 102. Then, the fixing plate 2 is released. The spring 204 will then generate tension, pushing the sliding block 208 to move until the fixing plate 2 moves above the gel plate 102 and the locking block 103. At this time, the snap-fit ​​plate 201 will also be inserted into the snap-fit ​​groove 207. At the same time, the snap-fit ​​plate 201 will be fitted onto both ends of the push plate 202. If the reagent bottle plate 101 needs to be removed later, simply move the moving fixing plate 2 away from the upper position of the adhesive plate 102 and the snap-fit ​​block 103. At this time, the snap-fit ​​plate 201 will move away from both ends of the push plate 202. Then, push the push plate 202 upward to remove a set of reagent bottle plates 101. By setting the fixing plate 2 to fix the two sides of the reagent bottle plate 101, and then removing the fixing plate 2 and the snap-fit ​​plate 201 at the same time later, the fixation of the reagent bottle plate 101 and the push plate 202 will be released, thereby pushing the push plate 202 to quickly and stably remove the reagent bottle plate 101, increasing the stability and convenience of using the enzyme-labeled plate.

[0028] In summary, compared with existing technologies, it has the following beneficial effects:

[0029] By moving the fixing plate 2 to both sides, the sliding block 208 and the internal compression spring 204 of the ELISA plate body 1 are pressed together. Then, the reagent bottle 101 is placed inside the ELISA plate body 1, and the fixing plate 2 is released. At this time, the spring 204 will generate tension to push the sliding block 208 to move. The fixing plate 2 moves to the position above the gel plate 102 and the snap-fit ​​block 103. At this time, the snap-fit ​​plate 201 will be sleeved on both ends of the push plate 202. If the reagent bottle 101 needs to be removed later, the fixing plate 2 and the snap-fit ​​plate 201 need to be moved. Then, the push plate 202 can be pushed upward to remove a set of reagent bottle 101. By setting the fixing plate 2 to fix the two sides of the reagent bottle 101, and simultaneously removing the fixing plate 2 and the snap-fit ​​plate 201 later, the fixing of the reagent bottle 101 and the push plate 202 is released, thereby pushing the push plate 202 to quickly and stably remove the reagent bottle 101, increasing the stability and convenience of using the ELISA plate.

[0030] The foregoing has shown and described the basic principles, main features, and advantages of this utility model. Those skilled in the art should understand that this utility model is not limited to the above embodiments. The embodiments and descriptions in the specification are merely illustrative of the principles of this utility model. Various changes and modifications can be made to this utility model without departing from its spirit and scope, and all such changes and modifications fall within the scope of the claims. The scope of protection of this utility model is defined by the appended claims and their equivalents.

Claims

1. A virus detection ELISA plate, comprising an ELISA plate body (1), wherein a reagent vial (101) is movably inserted into the interior of the ELISA plate body (1), characterized in that, The microplate body (1) is provided with a control mechanism on its exterior, the control mechanism including: A fixing plate (2) is movably disposed outside the body (1) of the enzyme labeling plate. The fixing plate (2) is movably snapped onto the outside of the reagent bottle plate (101). The fixing plate (2) is used to fix the position of the reagent bottle plate (101). A push plate (202) is movably disposed inside the body (1) of the enzyme labeling plate. The push plate (202) is disposed on the lower surface of the reagent bottle plate (101). The push plate (202) is used to push the reagent bottle plate (101) upward.

2. The virus detection ELISA plate according to claim 1, characterized in that: A connecting plate (203) is fixedly connected to the lower surface of the fixing plate (2), and the outside of the connecting plate (203) abuts against the outside of the enzyme labeling plate body (1).

3. The virus detection ELISA plate according to claim 2, characterized in that: The connecting plate (203) is fixedly connected to the outside of the snap-fit ​​plate (201), and the enzyme labeling plate body (1) is provided with a snap-fit ​​groove (207) on the outside. The push plate (202) is slidably connected to the inside of the snap-fit ​​groove (207), the snap-fit ​​plate (201) is movably inserted into the inside of the snap-fit ​​groove (207), and the snap-fit ​​plate (201) is movably snapped onto the outside of the push plate (202).

4. The virus detection ELISA plate according to claim 1, characterized in that: The reagent bottle plate (101) is fixedly connected to the outside of a snap-fit ​​block (103), and the enzyme label plate body (1) is fixedly connected to the outside of a glue plate (102). The snap-fit ​​block (103) is movably snapped into the inside of the glue plate (102), and the fixing plate (2) is slidably connected to the upper surface of the glue plate (102) and the snap-fit ​​block (103).

5. The virus detection ELISA plate according to claim 2, characterized in that: The enzyme labeling plate body (1) is internally fixedly connected to a limiting rod (205), and a sliding block (208) is movably sleeved on the outside of the limiting rod (205). A connecting rod (206) is fixedly connected to the outside of the sliding block (208). The connecting rod (206) is movably inserted into the inside of the enzyme labeling plate body (1), and the end of the connecting rod (206) is fixedly connected to the outside of the connecting plate (203).

6. The virus detection ELISA plate according to claim 5, characterized in that: The limiting rod (205) is externally movably sleeved with a spring (204), the spring (204) is fixedly connected to the outside of the sliding block (208), and the spring (204) is fixedly connected to the inside of the enzyme labeling plate body (1).

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