CN217997166U - Messenger mRNA active cell detection kit for preventing and treating pore enlargement - Google Patents
Messenger mRNA active cell detection kit for preventing and treating pore enlargement Download PDFInfo
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- CN217997166U CN217997166U CN202221716605.7U CN202221716605U CN217997166U CN 217997166 U CN217997166 U CN 217997166U CN 202221716605 U CN202221716605 U CN 202221716605U CN 217997166 U CN217997166 U CN 217997166U
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Abstract
The utility model relates to a cell detection field specifically is a messenger mRNA active cell detection box that prevention and cure pore is big, including detecting the box body, distinguishing mechanism and apron, the test tube groove has been seted up to the lateral wall on the detection box body, the test tube inslot portion inlays and is equipped with the test tube, the utility model discloses, examine time measuring to the mRNA cell that prevention and cure pore is big when needs, pour into the same sebum mRNA active cell of multiunit into the multiunit test tube in, then pour into different agents that restrain the sebum secretion grease into to each group's test tube in proper order into, pour into the different mRNA active cell's of all preparations into the in vitro into, rotate the apron through the hinge forward, make the sealing plug that the multiunit corresponds the rubber material of test tube position insert in the test tube mouth to make each group's test tube all obtain solitary sealed, avoided cross infection, improved the accuracy that detects the mRNA cell.
Description
Technical Field
The utility model relates to a cell detection field specifically is a messenger mRNA active cell detection box of prevention and cure pore is big.
Background
The gene is the largest determinant for determining the pore size, the sebaceous gland has a vigorous secretion, and researches indicate that the sebaceous gland secretion has a positive correlation with the pore size, and the hormone level has an important regulation effect on the sebaceous gland secretion, so that the pores of a male or a person with a vigorous grease secretion are relatively large, a special medicament is required to be used for suppressing the sebaceous gland secretion in the future, the activity of messenger mRNA in a plurality of groups of sebocytes needs to be detected in the production process of the medicament, the suppression effect on the sebaceous cell mRNA is detected by using different medicaments, and the detection needs to be performed by using a special mRNA cell detection kit.
The existing cell detection kit has some defects: in the messenger mRNA cell detection process, a plurality of groups of same mRNA cells are required to be injected into the test tube grooves of the detection box with the arrangement number, the situation of cross injection is easy to occur when a worker injects a detected inhibition reagent into a plurality of groups of arranged same existing mRNA cell test tube grooves for back and forth sampling, other reagents are repeatedly injected into the test tube grooves in which the reagents are injected, so that the detection result is in error, meanwhile, the existing cell detection box is only isolated from the outside air through the cover body, but the cover body is not provided with partitions, so that each reagent groove can be mutually polluted, and the error of the detection result is caused.
SUMMERY OF THE UTILITY MODEL
An object of the utility model is to provide a messenger mRNA activity cell detection box of prevention and cure pore size, a detection box test tube inslot for solve at present need inject the same mRNA cell of multiunit into the permutation number at the in-process that detects messenger mRNA cell, the staff will be surveyed and inhibited reagent and inject into the in-process of the same current mRNA cell test tube groove of multiunit permutation and appear the condition of cross injection easily when making a round trip to take a sample, other reagent of repeated injection in the test tube groove of injected reagent, cause the condition that the error appears in the testing result, the cell detection box that has now simultaneously only keeps apart through lid and outside air, thereby do not have between the lid and cut off between each reagent groove and can mutual contamination, cause the problem of testing result error.
Therefore, the utility model provides a messenger mRNA active cell detection box that prevention and cure pore is big, including detecting the box body, distinguishing mechanism and apron, the test tube groove has been seted up to the lateral wall on the detection box body, the test tube inslot portion inlays and is equipped with the test tube, the test tube lower extreme is provided with the distinguishing mechanism that is used for the effective difference of test tube to pouring into detect reagent and not pouring into detect reagent, the apron rotates the connection through the hinge and is lateral wall on the detection box body rear end, side surface fixed mounting has the sealing plug before the apron.
Preferably: distinguish the mechanism and include side channel, draw-in groove and flexible groove, the side channel is seted up at test tube groove right side wall, the inside fixed mounting of side channel has the slide bar, test tube right side fixed mounting has a lagging and cover to inlay at the slide bar outer wall, the first spring of lagging upper end fixedly connected with, the draw-in groove is seted up at test tube left end lateral wall, flexible groove is seted up in test tube groove left side, flexible inslot portion inlays and is equipped with the cardboard, the overhead gage has been seted up to flexible groove upper end, cardboard upper end fixed mounting has the arm-tie, arm-tie left end fixedly connected with second spring.
Preferably: the right side section of the clamping plate is the same as the section of the clamping groove in shape and is triangular.
Preferably, the following components: the front and back sizes of the pulling plate are matched with the front and back sizes of the top groove.
Preferably: the pulling plate is fixedly connected with one end of the second spring, and the other end of the second spring is fixedly connected with the side wall of the top groove.
Preferably: the lagging fixed connection one end of first spring, the other end fixed connection of first spring is at the side inslot wall.
Compared with the prior art, the beneficial effects of the utility model are that:
the utility model discloses, when needs examine time measuring to the mRNA cell of preventing and treating the pore size, with the same sebum mRNA active cell injection multiunit test tube of multiunit, then in proper order to each group in vitro the different reagent of sebum secretion of inhibition of injection, every press down the test tube to make it move in the test tube groove after accomplishing a set of test tube injection reagent, promote the inclined plane of cardboard downwards, pressure produces the component force left at the inclined plane thereby promote the cardboard left and make it move at flexible groove, it pushes the second spring extrusion to make its shrink and produce the potential energy to drive the arm-tie to move left at the top groove, the test tube moves down in the same direction of sleeve plate on the right side that drives the test tube, thereby produce obvious difference in height to the test tube in the test tube inslot embedding of this test tube and the test tube that has not been injected into the inhibition reagent still, the test tube has not obtained the independent mRNA sealed material of the test tube of the multiunit through the test tube of the mRNA sealed seal that the test tube had the cell of the crossing of the test tube that the messenger's reagent and injection reagent repeatedly injected into in-tube groove, thereby the test tube is not enough to have avoided the test tube to have the test tube to pass through the independent height difference of the mRNA sealed seal of the test tube that the messenger's the test tube that comes and has been injected into the test tube that the reagent of the test tube left side wall is opened and has been got into.
Drawings
FIG. 1 is a schematic perspective view of the present invention;
fig. 2 is a schematic front sectional view of the distinguishing mechanism of the present invention.
In the figure:
1. detecting the box body; 2. a test tube groove; 3. a test tube; 401. a side groove; 402. a slide bar; 403. sheathing; 404. a first spring; 405. a card slot; 406. a telescopic groove; 407. clamping a plate; 408. a top groove; 409. pulling a plate; 410. a second spring; 5. a cover plate; 6. and (4) sealing the plug.
Detailed Description
The technical solutions in the embodiments of the present invention will be described clearly and completely with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only 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 efforts all belong to the protection scope of the present invention.
Please refer to fig. 1-2, which are preferred embodiments of the present invention, a messenger mRNA active cell detecting box for preventing and treating large pores, comprising a detecting box body 1, a distinguishing mechanism and a cover plate 5, wherein a test tube slot 2 is disposed on the side wall of the detecting box body 1, a test tube 3 is embedded inside the test tube slot 2, the lower end of the test tube 3 is provided with the distinguishing mechanism for effectively distinguishing the test tube 3 which is injected with a detecting reagent and the test tube which is not injected with the detecting reagent, the cover plate 5 is rotatably connected to the side wall of the detecting box body 1 at the rear end through a hinge, and a sealing plug 6 is fixedly mounted on the front side surface of the cover plate 5.
The distinguishing mechanism comprises a side groove 401, a clamping groove 405 and a telescopic groove 406, wherein the side groove 401 is formed in the right side wall of the test tube groove 2, a sliding rod 402 is fixedly mounted inside the side groove 401, a sleeve plate 403 is fixedly mounted on the right side of the test tube 3 and sleeved on the outer wall of the sliding rod 402, a first spring 404 is fixedly connected to the upper end of the sleeve plate 403, the clamping groove 405 is formed in the side wall of the left end of the test tube 3, the telescopic groove 406 is formed in the left side of the test tube groove 2, a clamping plate 407 is embedded inside the telescopic groove 406, a top groove 408 is formed in the upper end of the telescopic groove 406, a pulling plate 409 is fixedly mounted at the upper end of the clamping plate 407, and a second spring 410 is fixedly connected to the left end of the pulling plate 409; when mRNA cells for preventing and treating large pores need to be detected, a plurality of groups of same sebum mRNA active cells are injected into a plurality of groups of test tubes 3, then different reagents for inhibiting sebum secretion grease are injected into each group of test tubes 3 in sequence, after the reagents are injected into one group of test tubes 3, the test tubes 3 are pressed downwards to move in the test tube grooves 2, the inclined surfaces of the clamping plates 407 are pushed downwards, leftward component force is generated by pressure on the inclined surfaces, the clamping plates 407 are pushed leftward to move in the telescopic grooves 406, the pulling plates 409 are driven to move leftward in the top grooves 408 to extrude the second springs 410 to contract to generate potential energy, meanwhile, the test tubes 3 move downwards to drive the sleeve plates 403 on the right side to move downwards along the sliding rods 402, so that the first springs 404 are stretched to generate potential energy, after the clamping grooves 405 formed in the left side walls of the test tubes 3 move to be aligned with the clamping plates, the second springs 410 release the potential energy to push the pulling plates 407 rightward to drive the clamping plates 407 to insert into the clamping grooves 405, so that the test tubes 3 and the operators cannot inject the reagents into the test tubes 3 repeatedly, and the mRNA active cells are injected into the test tubes 3, and the mRNA active reagents are not injected into the test tubes.
The right side of the clamping plate 407 has the same cross section as the clamping groove 405 and is triangular; the buckle is convenient to stabilize and the obvious distinguishing effect is achieved.
The front and rear dimensions of the pulling plate 409 are matched with the front and rear dimensions of the top groove 408; make buckle subassembly remove more stably.
The pulling plate 409 is fixedly connected with one end of a second spring 410, and the other end of the second spring 410 is fixedly connected with the side wall of the top groove 408; so as to efficiently distinguish the downward pressing of the test tube 3 filled with the inhibiting reagent.
The sleeve plate 403 is fixedly connected with one end of a first spring 404, and the other end of the first spring 404 is fixedly connected with the inner wall of the side groove 401; so as to efficiently distinguish the downward pressing of the test tube 3 filled with the inhibiting reagent.
The utility model discloses a work flow and principle: when mRNA cells for preventing and treating large pores are required to be detected, a plurality of groups of same sebum mRNA active cells are injected into a plurality of groups of test tubes 3, then different reagents for inhibiting sebum secretion grease are injected into each group of test tubes 3 in sequence, each time after the reagent is injected into one group of test tubes 3, the test tubes 3 are pressed downwards to move in the test tube grooves 2, the inclined surfaces of the clamping plates 407 are pushed downwards, leftward component force is generated by pressure on the inclined surfaces, so that the clamping plates 407 are pushed leftwards to move in the telescopic grooves 406, the pulling plates 409 are driven to move leftwards in the top grooves 408 to extrude the second springs 410 to generate potential energy, meanwhile, the test tubes 3 move downwards to drive the sleeve plates 403 on the right side to move downwards along the sliding rods 402, so that the first springs 404 are stretched to generate potential energy, after the clamping grooves 405 formed in the left side wall of the test tubes 3 move to be aligned with the clamping plates 407, the second spring 410 releases potential energy to push the pulling plate 409 to drive the clamping plate 407 to insert into the clamping groove 405, so that the height of the test tube 3 embedded in the test tube groove 2 is low compared with the height of the test tube 3 which is not injected with the inhibitory reagent, and an obvious height difference is generated between the test tube 3 and other test tubes 3, so that the worker can not repeatedly inject the inhibitory reagent into the same test tube 3 in the process of reciprocating the reagent and injecting the reagent, thereby avoiding distraction of the worker due to the need of memorizing the injection sequence, injecting different inhibitory reagents into the test tubes 3 of all prepared mRNA active cells, rotating the cover plate 5 forwards through the hinge, inserting the sealing plugs 6 made of rubber materials at the positions of the multiple groups of corresponding test tubes 3 into the tube ports of the test tubes 3, further leading each group of test tubes 3 to be individually sealed, and avoiding mutual cross infection.
The above description is for further details of the present invention, and it should not be assumed that the embodiments of the present invention are limited to these descriptions, and that a person of ordinary skill in the art to which the present invention pertains can make several simple deductions or substitutions without departing from the spirit of the present invention, and all should be considered as belonging to the protection scope defined by the claims submitted by the present invention.
Claims (6)
1. A messenger mRNA activity cell detection kit for preventing and treating pore enlargement, which is characterized in that: including detecting box body (1), distinguishing mechanism and apron (5), test tube groove (2) have been seted up to the lateral wall on detecting box body (1), test tube groove (2) inside inlays and is equipped with test tube (3), test tube (3) lower extreme is provided with the distinguishing mechanism that is used for injecting into detect reagent and effectively distinguishing test tube (3) that do not inject into detect reagent, apron (5) rotate the connection through the hinge and are detecting lateral wall on box body (1) rear end, apron (5) front side surface fixed mounting has sealing plug (6).
2. The cellular detection kit for messenger mRNA activity for preventing pore enlargement according to claim 1, wherein: distinguish the mechanism and include side groove (401), draw-in groove (405) and flexible groove (406), set up in test tube groove (2) right side wall side groove (401), the inside fixed mounting in side groove (401) has slide bar (402), test tube (3) right side fixed mounting has lagging (403) and cover to inlay at slide bar (402) outer wall, the first spring (404) of lagging (403) upper end fixedly connected with, set up in test tube (3) left end lateral wall draw-in groove (405), set up in test tube groove (2) left side flexible groove (406), flexible groove (406) inside is inlayed and is equipped with cardboard (407), top groove (408) have been seted up to flexible groove (406) upper end, cardboard (407) upper end fixed mounting has arm-tie (409), arm-tie (407) left end fixed connection has second spring (410).
3. The cellular detection kit for messenger mRNA activity for preventing pore enlargement according to claim 2, wherein: the right side cross-sectional shape of the clamping plate (407) is the same as the cross-sectional shape of the clamping groove (405), and the shapes of the clamping plate and the clamping groove are triangular.
4. The cellular detection kit for messenger mRNA activity for preventing pore enlargement according to claim 2, wherein: the front and back sizes of the pulling plate (409) are matched with those of the top groove (408).
5. The cell assay kit for messenger mRNA activity for preventing pore enlargement according to claim 2, wherein: the pulling plate (409) is fixedly connected with one end of a second spring (410), and the other end of the second spring (410) is fixedly connected with the side wall of the top groove (408).
6. The cellular detection kit for messenger mRNA activity for preventing pore enlargement according to claim 2, wherein: the sleeve plate (403) is fixedly connected with one end of a first spring (404), and the other end of the first spring (404) is fixedly connected with the inner wall of the side groove (401).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202221716605.7U CN217997166U (en) | 2022-07-05 | 2022-07-05 | Messenger mRNA active cell detection kit for preventing and treating pore enlargement |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202221716605.7U CN217997166U (en) | 2022-07-05 | 2022-07-05 | Messenger mRNA active cell detection kit for preventing and treating pore enlargement |
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| CN217997166U true CN217997166U (en) | 2022-12-09 |
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| CN202221716605.7U Active CN217997166U (en) | 2022-07-05 | 2022-07-05 | Messenger mRNA active cell detection kit for preventing and treating pore enlargement |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116297427A (en) * | 2023-03-10 | 2023-06-23 | 多莱泌生物科技(武汉)有限公司 | Exosome concentration detection kit |
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2022
- 2022-07-05 CN CN202221716605.7U patent/CN217997166U/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116297427A (en) * | 2023-03-10 | 2023-06-23 | 多莱泌生物科技(武汉)有限公司 | Exosome concentration detection kit |
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