Tissue culture flower rapid propagation induction device

Abstract

The utility model discloses a tissue culture flower rapid propagation induction device, and belongs to the technical field of flower planting. Comprising a bottom rod and multiple sets of culture plates, grooves are formed in the culture plates, limiting grooves are formed in the two sides of the grooves, the culture plates are slidably connected with a sliding plate through the limiting grooves, multiple sets of limiting pipes are evenly installed on the upper surface of the sliding plate, and a limiting assembly is installed in the center of the side face of the sliding plate. The tissue culture flower rapid propagation induction device has the beneficial effects that through arrangement of a limiting pipe, the limiting pipe provides limiting for a culture bottle, the situation that the culture bottle is touched and consequently the culture bottle falls off and is damaged is avoided, through arrangement of a limiting assembly, a sliding plate is conveniently limited, and when the sliding plate does not need to be pulled out, the sliding plate is fixed, so that the tissue culture flower rapid propagation induction device is convenient to use. Through sliding connection between the sliding plates and the culture plates, the sliding plates can be conveniently pulled out, the culture plates on the upper layer cannot hinder taking and placing of the culture bottles, and then the culture bottles can be conveniently taken and placed.

Description

Technical Field

[0001] The present application relates to the field of flower planting, and in particular to a tissue culture flower rapid propagation induction device. Background Art

[0002] Flower tissue culture refers to the process of culturing isolated flower organs, tissues, cells and protoplasts on an artificially prepared culture medium under sterile conditions and providing appropriate culture conditions to enable them to grow into complete plants. Flower tissue culture often uses an induction device to rapidly propagate the cultured flowers.

[0003] Under the prior art, flower tissues are placed in culture bottles, and then the culture bottles are placed in culture racks for culture to achieve rapid induced propagation. The culture racks are usually arranged in multiple layers. When it is necessary to take out the aged, blackened and dead flower tissue block culture bottles in the middle position of the middle-layer culture rack, the existing culture racks lack a mechanism for limiting the culture bottles. When taking out the culture bottles in the middle position of the middle-layer culture rack, it is easy to touch the other culture bottles, causing the culture bottles to fall and be damaged. In addition, when taking out the culture bottles in the middle position of the middle-layer culture rack, the upper-layer culture rack will hinder the taking-out action, which is inconvenient to operate, especially when the specifications of the culture bottles are large and the distance from the upper-layer culture rack is close. Therefore, a technical measure is proposed to solve the problem that there is no mechanism for limiting the culture bottles, and when taking out the culture bottles in the middle position of the middle-layer culture rack, it is easy to touch the other culture bottles, causing the culture bottles to fall and be damaged. In addition, when the specifications of the culture bottles are large and the distance from the upper-layer culture rack is close, it is inconvenient to take out the culture bottles in the middle position of the middle-layer culture rack. Utility Model Content

[0004] The content of this application is used to introduce concepts in a brief form, which will be described in detail in the detailed implementation section below. The content of this application is not intended to identify the key features or essential features of the technical solution claimed for protection, nor is it intended to limit the scope of the technical solution claimed for protection.

[0005] In order to solve the technical problems mentioned in the above background technology part, some embodiments of the present application provide a tissue culture flower rapid propagation induction device, including a bottom rod and a culture plate, wherein the culture plate is evenly arranged in multiple groups, a groove is opened in the culture plate, and limiting grooves are opened on both sides of the groove. The culture plate is slidably connected with a slide plate through the limiting grooves, and multiple groups of limiting tubes are evenly installed on the upper surface of the slide plate. A limiting assembly is installed at the center position of the side of the slide plate. Thanks to the sliding connection between the slide plate and the culture plate, the slide plate can be easily pulled out, and the upper culture plate will not hinder the taking and placing of the culture bottle, thereby facilitating the taking and placing of the culture bottle. At the same time, thanks to the setting of the limiting tube, the limiting tube provides a limit for the culture bottle to avoid touching the culture bottle and causing the culture bottle to fall and be damaged.

[0006] Furthermore, there are multiple groups of bottom rods, the sides of the bottom rods are connected to bottom plates, counterweights are movably placed in the bottom plates, the upper ends of the bottom rods are fixedly connected to the lower surfaces of the culture plates, and connecting rods are connected between the culture plates. Thanks to the setting of the counterweights, the culture rack is prevented from tipping over due to unstable center of gravity when the slide plate is pulled out.

[0007] Furthermore, two groups of symmetrically distributed magnets are installed on the side of the skateboard, and a pull ring is installed at a position of the skateboard close to the limiting component.

[0008] Furthermore, an iron sheet is provided on one side of the limiting groove close to the pull ring, the iron sheet is matched with the magnet, and the magnet is slidably matched with the limiting groove.

[0009] Furthermore, a lighting lamp is installed at the center of the lower surface of the culture plate. Thanks to the setting of the lighting lamp, on the one hand, it is convenient to observe the aging, blackening and dead flower tissues, and on the other hand, it can provide light for the photosynthesis of the flowers.

[0010] Furthermore, the limiting assembly includes a mounting plate, which is fixedly mounted on the lower surface of the skateboard. The side of the mounting plate is connected to a limiting block, and the limiting block is provided with a sliding groove. Thanks to the setting of the limiting assembly, it is convenient to limit the skateboard, and the skateboard can be fixed when it is not necessary to pull out the skateboard.

[0011] Furthermore, the limiting assembly also includes springs, which have two groups. The lower ends of the two groups of springs are fixedly installed below the inside of the limiting block. The upper ends of the springs are connected to pressure plates, which are slidably connected to the limiting block. A blocking block is connected to the center position of the upper surface of the pressure plate. A pull rod is installed at the center position of the lower surface of the pressure plate, which is slidably connected to the limiting block. A ring is connected to the lower end of the pull rod.

[0012] Furthermore, the clamping block is slidably matched with the sliding groove.

[0013] The utility model provides a limiting tube through the arrangement of the limiting tube, which provides a limiting position for the culture bottle, thereby preventing the culture bottle from being touched and falling and being damaged.

[0014] The setting of the limit assembly makes it convenient to limit the slide plate. When the slide plate does not need to be pulled out, the slide plate is fixed, and the downward pull ring drives the clamping block to move downward to release the limit on the side of the slide plate.

[0015] The sliding connection between the slide plate and the culture plate makes it easy to pull out the slide plate, and the upper culture plate will not cause any obstruction to the taking and placing of the culture bottles, thereby making it convenient to take and place the culture bottles. After releasing the limit on the slide plate through the limit assembly, use the pull ring to pull the slide plate outwards. When the magnets on both sides of the slide plate contact the iron sheet, the slide plate will no longer move, and the culture bottle can be placed in the limit tube. BRIEF DESCRIPTION OF THE DRAWINGS

[0016] The drawings constituting a part of this application are used to provide a further understanding of this application, so that other features, purposes and advantages of this application become more obvious. The illustrative embodiment drawings and their descriptions of this application are used to explain this application and do not constitute an improper limitation on this application.

[0017] In addition, throughout the drawings, the same or similar reference numerals represent the same or similar elements. It should be understood that the drawings are schematic and that the components and elements are not necessarily drawn to scale.

[0018] In the attached picture:

[0019] Figure 1 It is a schematic diagram of the structure of the utility model;

[0020] Figure 2 It is a structural schematic diagram of the culture plate and the slide plate being separated;

[0021] Figure 3 It is a schematic diagram of the side view structure of the culture plate;

[0022] Figure 4 This is a schematic diagram of the structure of the limit component in the separated state.

[0023] Reference numerals:

[0024] 1. Bottom rod; 2. Limiting assembly; 3. Bottom plate; 4. Counterweight; 5. Connecting rod; 6. Culture plate; 7. Slide plate; 8. Limiting groove; 9. Iron sheet; 10. Magnet; 11. Groove; 12. Limiting tube; 13. Pull ring; 14. Lighting lamp; 201. Limiting block; 202. Slide groove; 203. Block; 204. Press plate; 205. Spring; 206. Ring; 207. Pull rod; 208. Mounting plate. DETAILED DESCRIPTION

[0025] Embodiments of the present disclosure will be described in more detail below with reference to the accompanying drawings. Although certain embodiments of the present disclosure are shown in the accompanying drawings, it should be understood that the present disclosure can be implemented in various forms and should not be construed as being limited to the embodiments set forth herein. On the contrary, these embodiments are provided to provide a more thorough and complete understanding of the present disclosure. It should be understood that the drawings and embodiments of the present disclosure are only for exemplary purposes and are not intended to limit the scope of protection of the present disclosure.

[0026] It should also be noted that, for ease of description, only the parts related to the invention are shown in the drawings. In the absence of conflict, the embodiments and features in the embodiments of the present disclosure can be combined with each other.

[0027] It should be noted that the concepts such as "first" and "second" mentioned in the present disclosure are only used to distinguish different devices, modules or units, and are not used to limit the order or interdependence of the functions performed by these devices, modules or units.

[0028] It should be noted that the modifications of "one" and "plurality" mentioned in the present disclosure are illustrative rather than restrictive, and those skilled in the art should understand that unless otherwise clearly indicated in the context, it should be understood as "one or more".

[0029] The present disclosure will be described in detail below with reference to the accompanying drawings and in conjunction with embodiments.

[0030] Reference Figure 1 , Figure 2 , Figure 3 As shown, it includes a bottom rod 1 and a culture plate 6. The culture plate 6 is evenly provided with multiple groups. A groove 11 is opened in the culture plate 6. Limiting grooves 8 are opened on both sides of the groove 11. The culture plate 6 is slidably connected with a slide plate 7 through the limiting grooves 8. Multiple groups of limiting tubes 12 are evenly installed on the upper surface of the slide plate 7. A limiting component 2 is installed at the center position of the side of the slide plate 7. The bottom rod 1 has multiple groups. The side of the bottom rod 1 is connected to a bottom plate 3. A counterweight 4 is movably placed in the bottom plate 3. The upper end of the bottom rod 1 is fixedly connected to the lower surface of the culture plate 6. A connecting rod 5 is connected between the culture plates 6. Two groups of symmetrically distributed magnets 10 are installed on the side of the slide plate 7. A pull ring 13 is installed at the position of the slide plate 7 near the limiting component 2. The limiting groove 8 is close to the limit assembly 2. An iron sheet 9 is provided on one side of the pull ring 13, and the iron sheet 9 is adapted to the magnet 10, and the magnet 10 is slidably adapted to the limiting groove 8. A lighting lamp 14 is installed at the center position of the lower surface of the culture plate 6. The culture bottle is placed in the limiting tube 12 on the slide 7, and the limiting component 2 is used to release the limitation of the slide 7. When the magnets 10 on both sides of the slide 7 contact the iron sheet 9, the slide 7 no longer moves. At this time, the culture bottle is placed, and then the counterweight block 4 is placed in the bottom plate 3, and the lighting lamp 14 is started. When it is found that there is aged, blackened and dead floral tissue in the middle position of the middle layer culture plate 6, the limiting component 2 is repeated to release the limitation of the slide 7, the slide 7 is pulled out, the aged, blackened and dead floral tissue is taken out, and placed in a new culture bottle.

[0031] Reference Figure 1 , Figure 2 , Figure 4As shown, the limit assembly 2 includes a mounting plate 208, which is fixedly mounted on the lower surface of the slide plate 7, and the side of the mounting plate 208 is connected to the limit block 201, and the limit block 201 is provided with a slide groove 202. The limit assembly 2 also includes a spring 205, and the spring 205 has two groups. The lower ends of the two groups of springs 205 are fixedly mounted on the lower part of the limit block 201, and the upper ends of the springs 205 are connected to a pressing plate 204, and the pressing plate 204 is slidably connected to the limit block 201. The center position of the upper surface of the pressing plate 204 is connected to a card block 203, and the center position of the lower surface of the pressing plate 204 is installed with a pull rod 207, and the pull rod 207 is connected to the limit block 2 01 sliding connection, a ring 206 is connected to the lower end of the pull rod 207, and the block 203 is slidably adapted to the slide groove 202. The ring 206 is pulled downward, and the ring 206 moves downward to drive the pull rod 207 to move downward. The pull rod 207 moves downward to drive the pressure plate 204 to move downward. When the pressure plate 204 moves downward, the spring 205 is compressed. When the pressure plate 204 moves downward, it drives the block 203 to move downward. The block 203 moves downward to release the limitation on the side of the slide plate 7, and then the pull ring 13 is pulled to drive the slide plate 7 to move outward along the limiting groove 8. When the magnets 10 on both sides of the slide plate 7 contact the iron sheet 9, the slide plate 7 no longer moves.

[0032] Working principle: When conducting tissue culture on flowers, select a suitable culture bottle (commonly used ones are 100mL, 500mL, and 1L) according to the variety of flowers, inject suitable culture medium and inducer (culture medium provides energy for tissue growth, inducers are auxins and cytokinins, the main function of auxins is to induce callus formation and promote cell dedifferentiation, cytokinins mainly promote cell division and expansion, and induce bud differentiation), put the culture bottle into the limiting tube 12 on the slide 7 (the limiting tube 12 is set according to the size of the culture bottle, and the limiting tube 12 provides a limit for the culture bottle to avoid touching the culture bottle and causing the culture bottle to fall and be damaged), and use the limiting component 2 to release the limit on the slide 7 Specifically, the circular ring 206 is pulled downward, and the circular ring 206 moves downward to drive the pull rod 207 to move downward, and the pull rod 207 moves downward to drive the pressure plate 204 to move downward. When the pressure plate 204 moves downward, the spring 205 is compressed, and when the pressure plate 204 moves downward, the block 203 moves downward to release the limit on the side of the slide plate 7, and then the pull ring 13 is pulled to drive the slide plate 7 to move outward along the limit groove 8. When the magnets 10 on both sides of the slide plate 7 contact the iron sheet 9, the slide plate 7 no longer moves. At this time, the culture bottle is placed in it. Through the sliding connection between the slide plate 7 and the culture plate 6, the slide plate 7 is conveniently pulled out, and the upper culture plate 6 will not cause obstacles to the taking and placing of the culture bottle, thereby facilitating the taking and placing of the culture bottle;

[0033] Then, a counterweight 4 is placed on the bottom plate 3 (the counterweight 4 prevents the culture rack from tipping over due to unstable center of gravity when the slide plate 7 is pulled out), and the lighting lamp 14 is turned on. The lighting lamp 14 can be used to observe the aged, blackened and dead flower tissues, and can provide light for the photosynthesis of the flowers.

[0034] When aged, blackened and dead floral tissue is found in the middle of the middle layer culture plate 6, the limiting assembly 2 is repeated to release the limiting of the slide plate 7, the slide plate 7 is pulled out, the aged, blackened and dead floral tissue is taken out and put into a new culture bottle.

[0035] The above descriptions are only some preferred embodiments of the present disclosure and an explanation of the technical principles used. Those skilled in the art should understand that the scope of the invention involved in the embodiments of the present disclosure is not limited to the technical solutions formed by a specific combination of the above-mentioned technical features, but should also cover other technical solutions formed by any combination of the above-mentioned technical features or their equivalent features without departing from the above-mentioned inventive concept. For example, the above-mentioned features are replaced with the technical features with similar functions disclosed in the embodiments of the present disclosure (but not limited to) and the technical solutions formed.

Claims

1. A tissue culture flower rapid propagation induction device, comprising a bottom bar (1) and a culture plate (6), characterized in that: The culture plate (6) is evenly provided with a plurality of groups, a groove (11) is provided in the culture plate (6), and limiting grooves (8) are provided on both sides of the groove (11). The culture plate (6) is slidably connected to a slide plate (7) via the limiting grooves (8), a plurality of groups of limiting tubes (12) are evenly installed on the upper surface of the slide plate (7), and a limiting component (2) is installed at the center position of the side surface of the slide plate (7).

2. The tissue culture flower rapid propagation induction device according to claim 1, characterized in that: The bottom rod (1) has multiple groups, the side of the bottom rod (1) is connected to a bottom plate (3), a counterweight (4) is movably placed inside the bottom plate (3), the upper end of the bottom rod (1) is fixedly connected to the lower surface of the culture plate (6), and a connecting rod (5) is connected between the culture plates (6).

3. The tissue culture flower rapid propagation induction device according to claim 2, characterized in that: Two groups of symmetrically distributed magnets (10) are installed on the side of the slide plate (7), and a pull ring (13) is installed at a position of the slide plate (7) close to the limiting assembly (2).

4. The tissue culture flower rapid propagation induction device according to claim 3, characterized in that: An iron sheet (9) is provided on one side of the limiting groove (8) close to the pull ring (13); the iron sheet (9) is matched with the magnet (10); and the magnet (10) is slidably matched with the limiting groove (8).

5. The tissue culture flower rapid propagation induction device according to claim 4, characterized in that: An illuminating lamp (14) is installed at the center of the lower surface of the culture plate (6).

6. The tissue culture flower rapid propagation induction device according to claim 5, characterized in that: The limit assembly (2) comprises a mounting plate (208), wherein the mounting plate (208) is fixedly mounted on the lower surface of the slide plate (7), the side of the mounting plate (208) is connected to a limit block (201), and the limit block (201) is provided with a slide groove (202).

7. The tissue culture flower rapid propagation induction device according to claim 6, characterized in that: The limit assembly (2) also includes springs (205), and the springs (205) have two groups. The lower ends of the two groups of springs (205) are fixedly installed below the limit block (201). The upper ends of the springs (205) are connected to a pressure plate (204), and the pressure plate (204) is slidably connected to the limit block (201). The center position of the upper surface of the pressure plate (204) is connected to a clamping block (203). The center position of the lower surface of the pressure plate (204) is installed with a pull rod (207), and the pull rod (207) is slidably connected to the limit block (201). The lower end of the pull rod (207) is connected to a ring (206).

8. The tissue culture flower rapid propagation induction device according to claim 7, characterized in that: The clamping block (203) is slidably adapted to the sliding groove (202).

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