Sample Tube for Polymerase Chain Reaction and Polymerase Chain Reaction Device Thereof
20210394176 · 2021-12-23
Inventors
- Ying-Ta Lai (New Taipei City, TW)
- Yu-Cheng Ou (New Taipei City, TW)
- Jim-Yi Liao (New Taipei City, TW)
- Yi-Hsi Chen (New Taipei City, TW)
Cpc classification
G01N21/0303
PHYSICS
B01L3/5635
PERFORMING OPERATIONS; TRANSPORTING
B01L2300/0609
PERFORMING OPERATIONS; TRANSPORTING
B01L3/50851
PERFORMING OPERATIONS; TRANSPORTING
B01L2300/046
PERFORMING OPERATIONS; TRANSPORTING
B01L3/50825
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
The present invention provides a sample tube for polymerase chain reaction. The sample tube includes a sample tube body having an annular side wall and a bottom wall connected to annular side wall, wherein the annular side wall and the bottom wall form an accommodating space for accommodating a reaction mixture; and a first extension member extending from the bottom wall to the accommodating space, wherein, to carry out PCR, the reaction mixture immerses the first extension member, such that the light from the light source enters into the reaction mixture via the bottom and the bottom wall of the sample tube and the first extension member sequentially.
Claims
1. A sample tube for a polymerase chain reaction (PCR) , comprising: a sample tube body, having an annular side wall and a bottom wall connected to the annular side wall, wherein the annular side wall and the bottom wall form an accommodating space for accommodating a reaction mixture; and a first extension member, extending from the bottom wall to the accommodating space, wherein the reaction mixture immerses the first extension member during the PCR, such that a light beam of a light source enters the reaction mixture via the bottom and the bottom wall of the sample tube and the first extension member sequentially.
2. The sample tube of claim 1 further comprising: a sample tube cap, comprising a cover for sealing the accommodating space, and a second extension member extending from the cover, wherein the sample tube cap is inserted into the sample tube body, such that the second extension member is arranged to face the first extension member, and the reaction mixture exists between the first extension member and the second extension member.
3. The sample tube of claim 2, wherein the second extension member is made of an opaque material.
4. The sample tube of claim 3, wherein the first extension member has a first top surface, and the second extension member has a second top surface, there is a distance between the first top surface and the second top surface, and a liquid level of the reaction mixture is higher than a position of the second top surface in height.
5. The sample tube of claim 4, wherein the second top surface has an opaque property.
6. The sample tube of claim 2, wherein the second extension member is made of a transparent material.
7. The sample tube of claim 4, wherein the second extension member has a side wall in contact with the second top surface, and the side wall is arranged to face the annular side wall.
8. The sample tube of claim 7, wherein the side wall is arranged in parallel to the annular side wall.
9. The sample tube of claim. 4, wherein shapes of the first extension member and the second extension member are respectively one of a group of a cylinder, a trapezoidal cylinder, a rectangular cylinder and a cubic cylinder.
10. The sample tube of claim 2, wherein the second extension member comprises a neck and a shoulder, the neck is located between the cover and the shoulder and is connected to the cover and the shoulder, respectively, and the shoulder is arranged to face the first extension member.
11. The sample tube of claim 10, wherein after the sample tube cap seals the sample tube body, there is a gap between the shoulder and the annular side wall, and during the shoulder is inserted and in contact with the reaction mixture, a portion of the reaction mixture passes the gap and enters a space surrounded by the cover, the neck, the shoulder and the annular side wall.
12. The sample tube of claim 1, wherein the first extension member is made of a transparent material.
13. The sample tube of claim 1, wherein the bottom wall function as a converging lens.
14. The sample tube of claim 1, wherein the bottom wall and the first extension member are integrally formed, and a combination of the bottom wall and the first extension member can converge the light beam.
15. The sample tube of claim 1, wherein the first extension member is a light guiding member.
16. The sample tube of claim 2, wherein the sample tube cap and the sample tube body are integrally formed.
17. A sample tube, comprising: a sample tube body, having an accommodating space for accommodating a reaction mixture; and a first extension member, extending from a bottom of the sample tube body to the accommodating space, wherein a light beam of a light source enters the reaction mixture via the bottom and the first extension member sequentially.
18. The sample tube of claim 17 further comprising: a sample tube cap, comprising a cover for sealing the accommodating space, and a second extension member extending from the cover, wherein when the sample tube cap seals the sample tube body, and the second extension member is arranged to face the first extension member.
19. The sample tube of claim 18, wherein the second extension member is made of an opaque material.
20. The sample tube of claim 18, wherein the second extension member is made of a transparent material, and a second top surface of the second extension member has an opaque property.
21. The sample tube of claim 18, wherein when the second extension member is inserted into the sample tube body, the reaction mixture is distributed in an H shape in the sample tube as viewed from a side of the sample tube.
22. The sample tube of claim 18, wherein shapes of the first extension member and the second extension member are respectively one selected from the group consisting of a cylinder, a trapezoidal cylinder, a rectangular cylinder and a cubic cylinder.
23. The sample tube of claim 18, wherein the second extension member comprises a neck and a shoulder, and the neck is located between the cover and the shoulder and is connected to the cover and the shoulder, respectively.
24. The sample tube of claim 23, wherein there is a gap between the shoulder and the accommodating space, and a portion of the reaction mixture passes the gap and exists in a space surrounded by the cover, the neck, the shoulder and the annular side wall.
25. The sample tube of claim 17, wherein the first extension member is a light converging lens or a light guide cylinder.
26. The sample tube of claim 18, wherein a liquid level of the reaction mixture is in contact with a second top surface of the second extension member in the accommodating space.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0011]
[0012]
[0013]
DETAILED DESCRIPTION
[0014] Please refer to
[0015] In this structure, because the extension member 10 extends from the bottom of the sample tube body 2 to the accommodating space 5, such that the central portion of the bottom of the sample tube 1 is raised, thereby increasing the contact area between the annular side wall 3 of the sample tube 1 and the reaction mixture 12, so as to increase the ratio of the heating area of the sample tube 1 to the volume of the reaction mixture 12. As a result, in the present invention, the contact area between the annular side wall 3 and the reaction mixture 12 is increased because of the extension member 10, and thus the heating/cooling rate during denaturation, annealing, extension steps of each PCR cycle is increased, so as to further reduce the reaction time of the PCR, thereby substantially increasing heating and heat dissipation efficiency.
[0016] On the other hand, the sample tube 1 further includes a sample tube cap 6. The sample tube cap 6 includes a cover 7 for sealing the accommodating space 5 and an extension member 8 extending from the cover 7. The sample tube cap 6 is inserted into the sample tube body 2, such that the extension member 8 is arranged to face the extension member 10, and the reaction mixture 12 exists between the extension members 8 and 10. In detail, the extension member 10 has a top surface 11, and the extension member 8 has a top surface 9. There is a distance D ranged between the top surface 11 and the top surface 9, so that there is the reaction mixture 12 in between and the liquid level of the reaction mixture 12 is higher than the position of the top surface 9 in height, or the liquid level of the reaction mixture 12 is just in contact with the top surface 9. The extension member 8 has a side wall 13 in contact with the top surface 9, and the side wall 13 is arranged to face the annular side wall 3. It should be noted that the extension member 8 may be made of an opaque material, or the extension member 8 is made of a transparent material and the top surface 9 has an opaque property, so that the light beam of the light source enters the reaction mixture 12 via the bottom and the bottom wall 4 of the sample tube 1 and the extension member 10 sequentially without passing through the extension member 8. In addition, the side wall 13 and the annular side wall 3 are preferably arranged in parallel for ease of use (for example, it is convenient for the sample tube cap 6 having the cover 7 and the extension member 8 to be inserted into the sample tube body 2), but the side wall 13 and the annular side wall 3 can also be arranged to face each other by other methods. Sample tube cap 6 and sample tube body 2 may be integrally formed or may be two independent components. When being integrally formed, the sample tube cap 6 and the sample tube body 2 are connected with each other by a conventional linkage component (such as a plastic strip; not shown in
[0017] In this structure, because the extension member 10 extends from the bottom of the sample tube body 2 to the accommodating space 5, the extension member 8 extends from the cover 7, there is a reaction mixture 12 residing between the extension members 8 and 10, and the side walls 13 of the extension member 8 is arranged to face the annular side wall 3 when the sample tube cap 6 is inserted into the sample tube body 2. Therefore, when the extension member 8 is inserted into the sample tube body 2, the reaction mixture 12 is distributed in an H shape in the sample tube 1 as viewed from the side of the sample tube 1, thereby reducing the contact area between the reaction mixture 12 and air within the sample tube 1. As a result, in the present invention, the cover 7 is scaled up by configuring the extension member 8 (i.e. a plug) thereon to increase the contact area between the annular side wall 3 of the sample tube 1 and the reaction mixture 12, and to reduce the contact area between the reaction mixture 12 and air within the sample tube 1, so as to avoid bubble formation during the heating process of the PCR, disturbing optical signals and affecting the efficiency of the PCR.
[0018] It is worth noting that the main spirit of the present invention is to extend the bottom of the sample tube body 2 with the extension member 10 to increase the contact area between the sample tube body 2 and the reaction mixture 12, so as to improve heating and heat dissipation efficiency and reduce reaction time. Besides, the present invention may reduce the contact area between the reaction mixture 12 and air within the sample tube 1 by lengthening the cover 7 using the extension member 8 (i.e. a plug) , to avoid bubble formation. Those skilled in the art may make modifications or alterations accordingly, which are not limited thereto. For example, the sample tube 1 may be used for any PCR device and subjected to repetitively heating and cooling, but may also be used for other reactions. For instance, the sample tube 1 may be placed in a heater for warming or a water bath for thermostat reaction. Furthermore, the extension member 10 illustrated in
[0019] For example, please refer to
[0020] Specifically, the length of the neck 8a and the width of the shoulder 8b of the extension member 8′ (i.e. the plug) which extends from the cover 7 can be appropriately designed, so that during the sealing process of the sample tube cap 6 into the sample tube body 2, the gap d between the shoulder 8b and the annular side wall 3 gradually narrows to approach zero, and the sample tube body 2 is almost closed after sealing. In other words, during the sealing process of the sample tube cover 6 into the sample tube body 2 to gradually narrow gap d, gas (i.e., for venting) and the excess reaction mixture 12 are transferred to the space 15 where almost no reaction happened and no signals would be detected. As a result, via the appropriate structural design of the extension member 8′, the present invention may adaptively control the volume of the reaction mixture 12 for the temperature cycles of the PCR, to simultaneously improve the reaction efficiency and consistency of temperature control conditions, and reduce the disturbance of reaction and optical signal caused by the exposure to air.
[0021] In addition, please continuously refer to
[0022] In summary, the present invention elongates the bottom of the sample tube body 2 using the extension member 10, to increase the contact area between the annular side wall 3 and the reaction mixture 12, so as to increase the heating and heat dissipation efficiency and reduce the reaction time. Besides, by lengthening the cover 7 using the extension member 8 (i.e. a plug), the present invention may reduce the contact area between the reaction mixture 12 and the air, to avoid bubble formation. In addition, via the appropriate structural design of the extension member 8′, the present invention may control the volume of the reaction mixture 12 for reaction, and reduce the exposure to air. Furthermore, the bottom wall 4, the extension member 10 or the combination thereof converges or guides the light beam (excitation beam) of the light source, such that the present invention may reduce the optical noise in the optical path caused by the disturbance of the reaction mixture 12.
[0023] The sample tubes 1, 1′ disclosed, but not limited to, in the embodiments of the present invention are suitable for PCR devices compatible therewith, and are also suitable for PCR and quantitative analysis after DNA amplification using such PCR devices.
[0024] Those skilled in the art will readily observe that numerous modifications and alterations of the device and method may be made while retaining the teachings of the invention. Accordingly, the above disclosure should be construed as limited only by the metes and bounds of the appended claims.