CN215799502U - Fluorescent quantitative PCR detection sample cup structure - Google Patents
Fluorescent quantitative PCR detection sample cup structure Download PDFInfo
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- CN215799502U CN215799502U CN202121852620.XU CN202121852620U CN215799502U CN 215799502 U CN215799502 U CN 215799502U CN 202121852620 U CN202121852620 U CN 202121852620U CN 215799502 U CN215799502 U CN 215799502U
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Abstract
The utility model relates to a fluorescent quantitative PCR detection sample cup structure. The sample cup structure comprises a cup body and a cup cover, wherein a circular channel is arranged in the cup body, and the inner diameter of the inner wall of the channel is gradually reduced from the opening of the channel to the inner direction; the cup cover is provided with an elastic plug body, the plug body comprises a cup-shaped front plug and an annular rear plug, the outer wall of the front plug is provided with a taper, and the outer diameter of the outer wall of the opening end of the front plug is the largest; the outer wall of the rear plug is provided with an outward-opened annular skirt, and an acute included angle formed by the annular skirt and the outer wall of the rear plug faces the front plug; when the plug body is inserted into the channel from the opening of the channel, the outer wall of the front plug and the inner wall of the channel form compression seal, and the annular skirt and the inner wall of the channel form compression seal. According to the utility model, the double-sealing structure is formed by arranging the front plug and the rear plug on the cup cover and the channel of the cup body, so that liquid or gas leakage is avoided when high temperature is met, further pollution to the outside is avoided, the probability of accidents is reduced, and the safety is improved.
Description
Technical Field
The utility model relates to fluorescence detection, in particular to a fluorescent quantitative PCR detection sample cup structure.
Background
The real-time fluorescent quantitative PCR is characterized in that a fluorescent group is added in the PCR reaction, and the initial amount of a target gene is analyzed in real time by continuously monitoring the sequence of the occurrence of fluorescent signals and the change of the strength of the signals. Fluorescent quantitative PCR assays typically require the use of a sample cup to hold the sample to be assayed. The sample cup in the prior art is generally inserted and sealed by a cup cover at the opening of a cup body, but in the high-temperature process, the traditional structure has poor sealing property, so that sample gas leaks out, equipment and a laboratory are polluted, and even medical events are caused. The sealing structure of the sample cup is therefore to be improved.
SUMMERY OF THE UTILITY MODEL
The utility model aims to overcome the defects in the prior art and provides a fluorescent quantitative PCR detection sample cup structure to enhance the sealing performance.
In order to achieve the purpose, the utility model adopts the following technical scheme: a fluorescent quantitative PCR detection sample cup structure comprises a cup body and a cup cover, wherein a circular channel is arranged in the cup body, and the inner diameter of the inner wall of the channel is gradually reduced from the opening of the channel to the inner direction; the cup cover is provided with an elastic plug body, the plug body comprises a cup-shaped front plug and an annular rear plug, the outer wall of the front plug is provided with a taper, and the outer diameter of the outer wall of the opening end of the front plug is the largest; the outer wall of the rear plug is provided with an outward-opened annular skirt, and an acute included angle formed by the annular skirt and the outer wall of the rear plug faces the front plug; when the plug body is inserted into the channel from the opening of the channel, the outer wall of the front plug and the inner wall of the channel form compression seal, and the annular skirt and the inner wall of the channel form compression seal.
The cup cover is also provided with a snap ring, and the inner wall of the opening of the channel is provided with an annular clamping groove; when the plug body is inserted into the channel from the opening of the channel, the clamping ring is clamped in the clamping groove to form fixation.
One end of the cup cover is connected with the cup body through a connecting plate, and the cup cover, the cup body and the connecting plate are integrally formed through injection molding.
The bottom surface of the channel is an inclined surface.
The channel is provided with a containing cavity for containing samples below, and the channel is communicated with the containing cavity through two flow channels.
Compared with the prior art, the utility model has the beneficial effects that: the channel through stopper and back stopper and cup before the bowl cover sets up forms double seal structure, and sealing performance obtains the reinforcing, when meetting high temperature, liquid or gas leakage can not appear, and then can not pollute the external world, has reduced the probability of occurence of failure, has improved the security.
The foregoing description is only an overview of the technical solutions of the present invention, and in order to make the technical means of the present invention more clearly understood, the present invention may be implemented according to the content of the description, and in order to make the above and other objects, features, and advantages of the present invention more apparent, the following detailed description will be given of preferred embodiments.
Drawings
FIG. 1 is a sectional view of a structure of a sample cup according to the present invention (open state).
FIG. 2 is a sectional view of the structure of the specimen cup of the present invention (closed state).
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention will be described in detail with reference to the accompanying drawings and the detailed description.
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
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 and positional relationships based on those shown in the drawings, and are used only for convenience of description and simplicity of description, and do not indicate or imply that the device or element being referred to must have a particular orientation, be constructed and operated in a particular orientation, and thus, should not be considered 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 defined otherwise.
In the present invention, unless otherwise expressly stated or limited, "above" or "below" a first feature means that the first and second features are in direct contact, or that the first and second features are not in direct contact but are in contact with each other via another feature therebetween. 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.
In the description herein, references to the description of the term "one embodiment," "some embodiments," "an example," "a specific example," or "some examples," etc., mean that a particular feature, structure, material, or characteristic described in connection with the embodiment or example is included in at least one embodiment or example of the utility model. In this specification, the schematic representations of the terms used above should not be understood to necessarily refer to the same embodiment or example. Furthermore, the particular features, structures, materials, or characteristics described may be combined in any suitable manner in any one or more embodiments or examples. Furthermore, various embodiments or examples described in this specification can be combined and combined by one skilled in the art.
The present embodiment is a structure of a fluorescence quantitative PCR detection sample cup, and the specific structure is shown in fig. 1 and 2.
As shown in fig. 1 and 2, the sample cup structure comprises a cup body 10 and a cup cover 20. One end of the cup lid 20 is connected with the cup body 10 through a connecting plate 30, so that the cup lid 20 can be prevented from being lost. The other end of the cup cover 20 is a cover lifting sheet 201 for lifting the cup cover 20. The cup cover 20, the cup body 10 and the connecting plate 30 are integrally formed by injection molding, and the integral injection molding can improve the manufacturing efficiency and reduce the material types.
As shown in figures 1 and 2, a circular channel 11 is arranged in the cup body 10, and the inner diameter of the inner wall of the channel 11 is gradually reduced from the opening 111 of the channel 11 to the inner direction. The bottom surface 12 of the channel 11 is inclined. A cavity 14 for containing a sample is arranged below the channel 11, and the channel 11 is communicated with the cavity 14 through two flow channels 13.
As shown in fig. 1 and 2, the cap 20 has an elastic plug 202. The cup cover 20 is provided with a snap ring 21, and the inner wall of the opening 111 of the channel 11 is provided with an annular clamping groove 15. When the plug 202 is inserted into the channel 11 from the opening 111 of the channel 11, the snap ring 21 is snapped into the snap groove 15 to form a fixed position, so that the lid 20 cannot be easily separated from the channel 11 of the cup 10 to maintain the seal.
As shown in fig. 1 and 2, the plug body 202 includes a cup-shaped front plug 23 and an annular rear plug 22. The outer wall of the front plug 23 is tapered and the outer diameter of the outer wall of the open end of the front plug 23 is the largest. In fig. 2, the front plug 23 opens in the direction of the insertion channel 11. Further, the outer wall of the rear plug 22 is provided with an outwardly flared annular skirt 221. The skirt 221 forms an acute angle with the outer wall of the rear plug 22 towards the front plug 23. When the plug body 202 is inserted into the channel 11 from the opening 111 of the channel 11, the outer wall of the front plug 23 forms an interference compression seal with the inner wall of the channel 11, and the annular skirt 221 of the rear plug 22 forms an interference compression seal with the inner wall of the channel 11. At this time, the snap ring 21 is fixed in the clamping groove 15, the plug body 202 is fixed in the channel 11, two layers of sealing are always kept, and the sealing is not easy to lose efficacy. And because the diameter of the inner wall of the channel 11 is gradually reduced, the more the front plug 23 and the rear plug 22 are deeply arranged in the channel 11, the more the mutual pressing force is improved, and the sealing performance is stronger.
The sample cup structure of this embodiment forms double seal structure through setting up preceding stopper 23 and back stopper 22 and the passageway 11 of cup 10 at bowl cover 20, consequently when meetting high temperature, liquid or gas leakage can not appear, and then can not pollute the external world, has reduced the probability of occurence of failure, has improved the security.
The technical contents of the present invention are further illustrated by the examples only for the convenience of the reader, but the embodiments of the present invention are not limited thereto, and any technical extension or re-creation based on the present invention is protected by the present invention. The protection scope of the utility model is subject to the claims.
Claims (5)
1. A fluorescent quantitative PCR detection sample cup structure comprises a cup body and a cup cover, and is characterized in that a circular channel is arranged in the cup body, and the inner diameter of the inner wall of the channel is gradually reduced from the opening of the channel to the inner direction; the cup cover is provided with an elastic plug body, the plug body comprises a cup-shaped front plug and an annular rear plug, the outer wall of the front plug is provided with a taper, and the outer diameter of the outer wall of the opening end of the front plug is the largest; the outer wall of the rear plug is provided with an outward-opened annular skirt, and an acute included angle formed by the annular skirt and the outer wall of the rear plug faces the front plug; when the plug body is inserted into the channel from the opening of the channel, the outer wall of the front plug and the inner wall of the channel form compression seal, and the annular skirt and the inner wall of the channel form compression seal.
2. The structure of the fluorescence quantitative PCR detection sample cup as claimed in claim 1, wherein the cup cover is further provided with a snap ring, and the inner wall of the opening of the channel is provided with an annular clamping groove; when the plug body is inserted into the channel from the opening of the channel, the clamping ring is clamped in the clamping groove to form fixation.
3. The structure of the fluorescence quantitative PCR detection sample cup as claimed in claim 1, wherein one end of the cup cover is connected with the cup body through a connecting plate, and the cup cover, the cup body and the connecting plate are integrally formed by injection molding.
4. The structure of the fluorescence quantitative PCR detection sample cup of claim 1, wherein the bottom surface of the channel is an inclined surface.
5. The structure of the sample cup for fluorescence quantitative PCR detection according to claim 1, wherein a cavity for containing the sample is arranged below the channel, and the channel is communicated with the cavity through two flow channels.
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CN202121852620.XU CN215799502U (en) | 2021-08-09 | 2021-08-09 | Fluorescent quantitative PCR detection sample cup structure |
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CN202121852620.XU CN215799502U (en) | 2021-08-09 | 2021-08-09 | Fluorescent quantitative PCR detection sample cup structure |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN114689128A (en) * | 2022-05-31 | 2022-07-01 | 青岛道万科技有限公司 | Special temperature and pressure measuring instrument and method thereof |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN114689128A (en) * | 2022-05-31 | 2022-07-01 | 青岛道万科技有限公司 | Special temperature and pressure measuring instrument and method thereof |
CN114689128B (en) * | 2022-05-31 | 2022-08-19 | 青岛道万科技有限公司 | Special temperature and pressure measuring instrument and method thereof |
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