CN212922539U

CN212922539U - Kanamycin ELISA (enzyme-linked immuno sorbent assay) detection kit

Info

Publication number: CN212922539U
Application number: CN202021507354.2U
Authority: CN
Inventors: 常滨滨; 杨泽正
Original assignee: Tianjin Yifan Biotechnology Co ltd
Current assignee: Tianjin Yifan Biotechnology Co ltd
Priority date: 2020-07-27
Filing date: 2020-07-27
Publication date: 2021-04-09
Anticipated expiration: 2030-07-27

Abstract

The utility model provides a kanamycin ELISA detect reagent box belongs to detect reagent box technical field. The kanamycin ELISA detection kit comprises a shell and a placement component. The shell comprises a box body and a box cover. The placing assembly comprises a fixing block, a placing frame, a buffer layer, a spring piece, a limiting plate, a top cover and a limiting block. During the use, anticlockwise rotate the lid 90, the spring part drives the limiting plate thereupon and releases the spout with the stopper, can take off the lid, puts into the reagent bottle, puts into the rack back to the reagent bottle, stretches into the spout with the stopper of lid bottom from the rack top, clockwise rotates 90 and loosens the lid again, and the spring part drives the limiting plate thereupon and supports the stopper tightly in the spout to the completion is spacing to the lid. The utility model discloses convenient to use when playing good guard action to the reagent bottle, can effectively avoid frequently opening and close to cause the pollution to the reagent bottle.

Description

Kanamycin ELISA (enzyme-linked immuno sorbent assay) detection kit

Technical Field

The utility model relates to a detect reagent box technical field particularly, relate to kanamycin ELISA detect reagent box.

Background

The detection kit is a packing carton that holds detect reagent, holds multiple detect reagent in the reagent box, and the detection kit can protect these detect reagent, prevents that these detect reagent from carrying the in-process of transportation impaired. Test kits are commonly available for use in hospitals and pharmaceutical enterprises.

At present, when the existing detection kit is used, reagent bottles are directly clamped on a multi-hole plate in the kit, the tops of the reagent bottles are directly exposed outside, and the surfaces of other reagent bottles can be polluted by frequently opening the kit and taking and placing the reagent bottles.

SUMMERY OF THE UTILITY MODEL

In order to compensate above not enough, the utility model provides a kanamycin ELISA detect reagent box aims at improving the problem that can cause the pollution to other reagent bottle surfaces when current detect reagent box frequently opens.

The utility model discloses a realize like this:

the utility model provides a kanamycin ELISA detect reagent box, include the shell and place the subassembly.

The shell includes box body and lid, lid one side with box body top one side is articulated, the lid opposite side with box body opposite side joint.

The placing assembly comprises a fixing block, a placing frame, a buffer layer, a spring part, a limiting plate, a top cover and a limiting block, wherein the placing frame is embedded in the fixing block, the buffer layer is fixed on the inner wall of the placing frame, a sliding groove is formed in the placing frame, grooves are formed in the bottoms of the two ends of the sliding groove, the bottom of the spring part is fixedly connected with the bottom of the groove, the lower surface of the limiting plate is fixedly connected with the top of the spring part, the limiting block is fixed to the bottom of the top cover, and the limiting.

In an embodiment of the present invention, the housing further includes an articulated element, the lid passes through on one side the articulated element with box body top one side is rotated and connected.

In an embodiment of the present invention, the chute end is fixed with a first cushion pad.

In an embodiment of the present invention, the buffer layer includes a second buffer pad and a third buffer pad, the second buffer pad is fixed on the inner wall of the rack, and the third buffer pad is fixed on the second buffer pad.

The utility model discloses an in one embodiment, the spring part includes guide pin bushing, spring and slide bar, the guide pin bushing bottom with recess bottom fixed connection, the slide bar bottom is passed through the spring with guide pin bushing inner wall connection.

The utility model discloses an in one embodiment, the top cap includes lid and antiskid cover, antiskid cover is established on the lid.

The utility model discloses an in one embodiment, the top cap still includes the buffer block, the buffer block is fixed lid inner wall top.

The utility model discloses an in one embodiment, the stopper includes fixed plate and block, the block lateral part passes through the fixed plate with lid bottom fixed connection.

In an embodiment of the present invention, the placing assembly further includes a dehumidifying part, and the dehumidifying part is disposed on the inner wall of the box body.

The utility model discloses an in the embodiment, the dehumidification piece is including fixed frame and dehumidification piece, fixed frame is fixed the box body inner wall, the dehumidification piece sets up in the fixed frame.

The utility model has the advantages that: the utility model discloses a kanamycin ELISA detect reagent box that above-mentioned design obtained, during the use, anticlockwise rotates the lid 90, and the spring part drives the limiting plate thereupon and releases the spout with the stopper, can take off the lid, puts into the reagent bottle, puts into the rack back to the reagent bottle, stretches into the spout with the stopper of lid bottom from the rack top in, clockwise rotation 90 loosens the lid again, and the spring part drives the limiting plate thereupon and supports tightly in the spout with the stopper to accomplish the spacing to the lid. The utility model discloses convenient to use when playing good guard action to the reagent bottle, can effectively avoid frequently opening and close to cause the pollution to the reagent bottle.

Drawings

In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings that are required to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present invention, and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained according to the drawings without inventive efforts.

FIG. 1 is a schematic diagram of a kanamycin ELISA test kit provided by an embodiment of the present invention;

fig. 2 is a schematic structural diagram of a housing according to an embodiment of the present invention;

fig. 3 is a schematic structural diagram of a placement module according to an embodiment of the present invention;

fig. 4 is an enlarged schematic structural diagram of a point a in fig. 3 according to an embodiment of the present invention;

fig. 5 is a schematic structural diagram of a top cover and a limiting block provided by the embodiment of the present invention;

fig. 6 is a schematic view of a second perspective structure of the placement frame according to an embodiment of the present invention.

In the figure: 100-a housing; 110-a cartridge; 120-box cover; 130-a hinge; 200-placing the assembly; 210-fixed block; 220-placing the rack; 221-a chute; 222-a groove; 223-a first cushion; 230-a buffer layer; 231-a second cushion; 232-a third cushion; 240-spring element; 241-guide sleeve; 242-a spring; 243-a slide bar; 250-a limiting plate; 260-a top cover; 261-a cover; 262-antiskid sleeve; 263-buffer block; 270-a limiting block; 271-a fixed plate; 272-block; 280-a dehumidifying part; 281-fixing frames; 282-dehumidification block.

Detailed Description

To make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the drawings of the embodiments of the present invention are combined to clearly and completely describe the technical solutions of the embodiments of the present invention, and obviously, the described embodiments are some embodiments of the present invention, not all embodiments. Based on the embodiments in the present invention, all other embodiments obtained by a person skilled in the art without creative work belong to the protection scope of the present invention.

Thus, the following detailed description of the embodiments of the present invention, presented in the accompanying drawings, is not intended to limit the scope of the invention, as claimed, but is merely representative of selected embodiments of the invention. Based on the embodiments in the present invention, all other embodiments obtained by a person skilled in the art without creative work belong to the protection scope of the present invention.

It should be noted that: like reference numbers and letters refer to like items in the following figures, and thus, once an item is defined in one figure, it need not be further defined and explained in subsequent figures.

In the description of the present invention, it is to be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and to simplify the description, but do not indicate or imply that the device or element referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore should not be construed as limiting the present invention.

Furthermore, the terms "first", "second" and "first" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly indicating the number of technical features indicated. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of the present invention, "a plurality" means two or more unless specifically limited otherwise.

In the present invention, unless otherwise expressly stated or limited, the terms "mounted," "connected," and "fixed" are to be construed broadly and may, for example, be fixedly connected, detachably connected, or integrally formed; either directly or indirectly through intervening media, either internally or in any other relationship. The specific meaning of the above terms in the present invention can be understood according to specific situations by those skilled in the art.

In the present disclosure, unless expressly stated or limited otherwise, the first feature "on" or "under" the second feature may comprise direct contact between the first and second features, or may comprise contact between the first and second features not directly. Also, the first feature being "on," "above" and "over" the second feature includes the first feature being directly on and obliquely above the second feature, or merely indicating that the first feature is at a higher level than the second feature. A first feature being "under," "below," and "beneath" a second feature includes the first feature being directly under and obliquely below the second feature, or simply meaning that the first feature is at a lesser elevation than the second feature.

Examples

Referring to fig. 1-6, the present invention provides a technical solution: kanamycin ELISA detect reagent box, including shell 100 with place subassembly 200, place subassembly 200 and set up inside shell 100, can deposit the reagent bottle of its inside and fix and protect effectively.

Referring to fig. 2, the housing 100 includes a box body 110 and a box cover 120, one side of the box cover 120 is hinged to one side of the top of the box body 110, the other side of the box cover 120 is fastened to the other side of the box body 110, the housing 100 further includes a hinge 130, and one side of the box cover 120 is rotatably connected to one side of the top of the box body 110 through the hinge 130.

Referring to fig. 3 to 6, the placing assembly 200 includes a fixing block 210, a placing frame 220, a buffer layer 230, a spring element 240, a limiting plate 250, a top cover 260 and a limiting block 270, the placing frame 220 is embedded in the fixing block 210, the buffer layer 230 is fixed on the inner wall of the placing frame 220, the buffer layer 230 includes a second buffer pad 231 and a third buffer pad 232, the second buffer pad 231 is a rubber pad, the third buffer pad 232 is a sponge pad, the second buffer pad 231 is fixed on the inner wall of the placing frame 220, the third buffer pad 232 is fixed on the second buffer pad 231, so that the buffer function of damping during collision can be achieved, the protection effect of the reagent bottle is improved, the placing frame 220 is provided with a sliding groove 221, the bottom of each of the two ends of the sliding groove 221 is provided with a groove 222, the bottom of the spring element 240 is fixedly connected with the bottom of the groove, The bottom of the guide sleeve 241 is fixedly connected with the bottom of the groove 222, the bottom end of the sliding rod 243 is connected with the inner wall of the guide sleeve 241 through the spring 242, and the lower surface of the limiting plate 250 is fixedly connected with the top of the spring part 240.

It should be specifically noted that the limiting block 270 is fixed at the bottom of the top cover 260, the top cover 260 includes a cover body 261 and an anti-slip sleeve 262, the anti-slip sleeve 262 is a rubber sleeve, the anti-slip sleeve 262 is sleeved on the cover body 261 to facilitate rotation of the cover body 261, the limiting block 270 slides in the sliding groove 221, the top cover 260 further includes a buffering block 263, the buffering block 263 is a sponge block, the buffering block 263 is fixed at the top of the inner wall of the cover body 261 to enable the top of the reagent bottle to flexibly contact with the inner wall of the cover body 261, the end of the sliding groove 221 is fixed with a first buffering pad 223, the first buffering pad 223 is a sponge pad to enable the limiting block 270 to flexibly contact with the end of the sliding groove 221, the limiting block 270 includes a fixing plate 271 and a block 272, the side of the block 272 is fixedly connected with the bottom of the cover body 261 through the fixing plate 271, the placing assembly 200, the dehumidifying part 280 comprises a fixing frame 281 and a dehumidifying block 282, the dehumidifying block 282 is a water-absorbing resin block, the fixing frame 281 is fixed on the inner wall of the box body 110, the fixing frame 281 is a porous frame, the dehumidifying block 282 is arranged in the fixing frame 281, moisture in the box body 110 can be removed, after reagent bottles are placed in the placing frame 220, a limiting block 270 at the bottom of the cover body 261 extends into the sliding groove 221 from the top of the placing frame 220, the cover body 261 is loosened by clockwise rotation for 90 degrees, the spring part 240 drives the limiting plate 250 to abut against the limiting block 270, so that limiting of the cover body 261 is completed, when the reagent bottles are taken out, the cover body 261 is rotated for 90 degrees counterclockwise, the spring part 240 drives the limiting plate 250 to push the limiting block 270 out of the sliding groove 221, the cover body 261 can be taken out, and.

Specifically, the working principle of the kanamycin ELISA detection kit is as follows: during the use, anticlockwise rotate lid 261 90, spring part 240 drives limiting plate 250 thereupon and pushes out the spout 221 with stopper 270, can take off lid 261, puts into the reagent bottle, puts into rack 220 the back to the reagent bottle, stretches into spout 221 with the stopper 270 of lid 261 bottom from the rack 220 top, clockwise rotation 90 loosens lid 261 again, and spring part 240 drives limiting plate 250 thereupon and supports stopper 270 tightly to accomplish the spacing to lid 261.

The above is only a preferred embodiment of the present invention, and is not intended to limit the present invention, and various modifications and changes will occur to those skilled in the art. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims

1. The kanamycin ELISA detection kit is characterized by comprising

The shell (100) comprises a box body (110) and a box cover (120), one side of the box cover (120) is hinged with one side of the top of the box body (110), and the other side of the box cover (120) is clamped with the other side of the box body (110);

place subassembly (200), place subassembly (200) including fixed block (210), rack (220), buffer layer (230), spring part (240), limiting plate (250), top cap (260) and stopper (270), rack (220) inlay and establish in fixed block (210), buffer layer (230) are fixed rack (220) inner wall, spout (221) have been seted up on rack (220), spout (221) both ends bottom all is seted up fluted (222), spring part (240) bottom with recess (222) bottom fixed connection, stopper (250) lower surface with spring part (240) top fixed connection, stopper (270) are fixed top cap (260) bottom, stopper (270) in slide in spout (221).

2. The kanamycin ELISA test kit of claim 1 wherein the housing (100) further comprises a hinge (130), and wherein one side of the lid (120) is pivotally connected to one side of the top of the case (110) via the hinge (130).

3. The kanamycin ELISA test kit of claim 1 wherein a first bumper pad (223) is affixed to the end of the chute (221).

4. The kanamycin ELISA test kit of claim 1, wherein the buffer layer (230) comprises a second buffer (231) and a third buffer (232), the second buffer (231) is fixed on the inner wall of the rack (220), and the third buffer (232) is fixed on the second buffer (231).

5. The kanamycin ELISA test kit of claim 1 wherein the spring element (240) comprises a guide sleeve (241), a spring (242) and a slide bar (243), the bottom of the guide sleeve (241) is fixedly connected with the bottom of the groove (222), and the bottom end of the slide bar (243) is connected with the inner wall of the guide sleeve (241) through the spring (242).

6. The kanamycin ELISA test kit of claim 1 wherein the cap (260) comprises a cap (261) and an anti-slip cover (262), the anti-slip cover (262) is sleeved on the cap (261).

7. The kanamycin ELISA test kit of claim 6 wherein the top cover (260) further comprises a buffer block (263), wherein the buffer block (263) is fixed to the top of the inner wall of the cover (261).

8. The kanamycin ELISA test kit of claim 6, wherein the stopper (270) comprises a fixing plate (271) and a block (272), and the side of the block (272) is fixedly connected with the bottom of the cover (261) through the fixing plate (271).

9. The kanamycin ELISA test kit of claim 1 wherein the placement module (200) further comprises a desiccant (280), the desiccant (280) being disposed on the inner wall of the cartridge body (110).

10. The kanamycin ELISA test kit of claim 9 wherein the desiccant (280) comprises a fixed frame (281) and a desiccant block (282), the fixed frame (281) is fixed on the inner wall of the cartridge body (110), and the desiccant block (282) is disposed in the fixed frame (281).