Microsatellite instability multiple detection system and kit
An unstable and multiple detection technology, which is applied in the determination/testing of microorganisms, biochemical equipment and methods, etc., can solve the problems that the advantages of multiple PCR experiments cannot be used, there is not enough clinical data support, and the cost of experiments is high. It is conducive to standardized operation, convenient for large-scale promotion and application, and intuitive effect of PCR result analysis
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Embodiment 1
[0039] 1. The composition of the kit.
[0040] The microsatellite instability detection kit of the present embodiment comprises PCR reaction solution, primer mixture, hot start enzyme, positive control solution and negative control solution, PCR reaction solution, primer mixture, hot start enzyme, positive control solution and negative control solution The control solutions were placed in different test tubes, as shown in Table 1.
[0041] Table 1 Kit composition table
[0042]
[0043] The PCR reaction solution is prepared from 10×PCR buffer, dNTPs and hot-start enzyme. 10×PCR buffer includes 100mM Tris-HCl, 500mM KCl and 15mM MgCl 2 , the pH value of the Tris-HCl buffer used to configure the PCR buffer is 8.3. dNTPs include dATP, dGTP, dCTP and dTTP, the concentration of dATP, dGTP, dCTP and dTTP is 2.5mM, and the final concentration in the reaction system is 0.2mM. The hot start enzyme uses TaqDNA polymerase at a concentration of 5U / μl, and the final concentration in...
Embodiment 2
[0086] The rest of the microsatellite instability detection kit of this embodiment is the same as that of Example 1, except that the PCR reaction solution and the primer mixture are mixed together in advance and placed in the same test tube.
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