1. Field of the Invention
The present invention relates generally to apparatuses for use in polymerase chain reaction (hereinafter referred to as “PCR”) and more particularly, to an apparatus for holding a test tube for insulated isothermal PCR.
2. Description of the Related Art
In the filed of biotechnology, polymerase chain reaction (PCR) is a well-known technology used to amplify specific nucleic acid sequences. The PCR process comprises three major steps including denaturation, primer annealing and extension, which require different reaction temperatures. The required temperature for the denaturation step is typically in a range between 90° C. and 97° C. The required temperature for the primer annealing step will depend on the melting temperature of the primer used. Typically, the annealing temperature ranges from 35° C. to 65° C. The required temperature for the extension step is typically about 72° C.
The insulated isothermal PCR is based on Rayleigh-Bénard convection, which is driven by buoyancy when heating fluid layer from below, is a common physical phenomenon. The insulated isothermal PCR is generally performed by immersing the bottom of a test tube which contains a reaction mixture into a hot water in such a way that the rest portion of the test tube is exposed to atmosphere at room temperature for heat dissipation. As a result, the temperature of the reaction mixture will gradually decrease from the bottom of the reaction mixture having a temperature of about 97° C. toward the liquid level of the reaction mixture having a temperature of about 35° C. Because of the temperature gradient, the heat convection is induced, such that the reaction mixture will flow through various regions having different temperatures and then undergo different reaction steps.
In the conventional apparatus for performing a convection PCR, because the portion of the test tube, which is exposed to the ambient air at room temperature for heat dissipation, has a low heat dissipating rate, the temperature at the liquid level of the reaction mixture will become higher and higher due to the increment of the heating time. As a result, the temperature at the liquid level of the reaction mixture may rise to a degree higher than the required temperature suitable for conducting the primer annealing step before the convection PCR has been performed completely. Under this circumstance, the polymerase chain reaction may break, such that a desired, large amount of copies of specific nucleic acid sequences may not be obtained.
The present invention has been accomplished in view of the above-noted circumstances. It is the primary objective of the present invention to provide an apparatus for insulated isothermal PCR, which can ensure that the temperature at the liquid level of the reaction mixture is lower than the temperature suitable for conducting the primer annealing step in the PCR process.
To achieve the above-mentioned objective, the apparatus provided by the present invention is adapted for holding a test tube in which a insulated isothermal polymerase chain reaction is performed, which comprises a heat sink having a main body provided with a through hole for insertion of the test tube. The through hole has a relatively big diameter section and a relatively small diameter section located below the relatively big diameter section. By means of the design of the present invention, the temperature at the liquid level of the reaction mixture can be kept in a degree lower than the temperature suitable for conducting the primer annealing step in the PCR process.
The present invention will become more fully understood from the detailed description given herein below and the accompanying drawings which are given by way of illustration only, and thus are not limitative of the present invention, and wherein:
As shown in
In order to stably mount the test tube 12 in the heat sink 20, the tube rack 30 can be further provided on the heat sink 20. The tube rack 30 is provided with a receiving hole 32 for insertion of the test tube 12 to stably position the test tube 12, thereby preventing the outer wall surface of the test tube 12 from contacting the wall surface of the through hole 24 of the heat sink 20 so as to avoid that the temperature of the reaction mixture drops too quickly.
In practice, the receiving hole 32 of the tube rack 30 may be configured, in succession order from a top thereof toward a bottom thereof, a relatively big diameter section 321, a shoulder 322 and a relatively small diameter section 323, in which the shoulder 322 is adapted for stopping a shoulder 121 of the test tube 12 such that the test tube 12 can be stably positioned. In addition, a support seat 40 is provided below the heat sink 20. The bottom 124 of the test tube 12 is heated by a heat source (not shown in the drawings) to keep the temperature of the reaction mixture of PCR inside the bottom 124 in a range about 90° C. to 97° C.
Further, the bottom end 301 of the tube rack 30 is inserted into the through hole 24 of the heat sink 20, such that the tube rack 30 is stably mounted on the heat sink 20.
Furthermore, in the preferred embodiment of the present invention, the diameter of the relatively small diameter section 242 of the through hole 24 is configured to gradually and downwardly decrease. According to many experiments and modifications, it is found that using this configuration to dissipate heat can yield a highest reaction efficiency of PCR. The aforesaid experiments for PCR were conducted in seven different environmental temperatures ranging from 10° C. to 40° C. with a condition that the reaction mixture inside the bottom 124 of the test tube 12 was heated to 93° C. to 97° C. The temperature of the heat sink 20 measured ranges from 36° C. to 53° C., and the temperature at the reaction mixture level measured ranges from 36° C. to 53° C.; therefore, the PCR is performed smoothly.
The invention being thus described, it will be obvious that the same may be varied in many ways. For example, as shown in
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100109780 A | Mar 2011 | TW | national |
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Number | Date | Country | |
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20120244048 A1 | Sep 2012 | US |