Primer group and method for identifying dendrobium huoshanense and dendrobium officinale product based on Real-time ARMS-qPCR
A technology of Dendrobium huoshanense and identification method, which is applied in the fields of biochemical equipment and methods, DNA/RNA fragments, recombinant DNA technology, etc., can solve the problems of low accuracy, poor repeatability, and long time, and achieve the effect of accurate identification
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Embodiment 1
[0043](1) Select Dendrobium Huoshanense, Dendrobium slender stems, Dendrobium officinale and other 17 species of Dendrobium spp. (as shown in Table 1), grind the samples to be tested fully with liquid nitrogen, and extract total DNA respectively. The extraction method is the improved CTAB extraction method developed. Compared with the traditional CTAB method, the improved CTAB method increases the amount of CTAB and PVP40 by 3 times;
[0044] (2) Using the above-mentioned dendrobium sample DNA as a template, utilize Seq ID NO.1 and 2 to carry out pre-amplification to obtain pre-amplified DNA, which can improve the concentration of template DNA to be identified;
[0045] The pre-amplification reaction was performed on a PCR machine: Veriti 96Well Thermal Cycler (Applied Biosystems);
[0046] The characteristics of the PCR reaction system are: the total volume is 20 μL, which contains: 10×PCR Buffer 2 μL, dNTP (10 mmol L -1 ) 1.4 μL, Mg 2+ (25mmol·L -1 ) 1.4 μL, preamplified ...
Embodiment 2
[0061] (1) Select Dendrobium Huoshanense, Dendrobium slender stems, Dendrobium candidum and other 17 kinds of Dendrobium samples (same as Example 1), fully grind the samples to be tested with liquid nitrogen, and use the improved CTAB method to extract the total DNA respectively;
[0062] (2) Using the above-mentioned dendrobium sample DNA as a template, utilize Seq ID NO.3 and 4 to carry out pre-amplification to obtain pre-amplified DNA, which can improve the concentration of template DNA to be identified;
[0063] The pre-amplification reaction was performed on a PCR machine: Veriti 96 Well Thermal Cycler (Applied Biosystems);
[0064] The characteristics of the PCR reaction system are: the total volume is 20 μL, which contains: 10×PCR Buffer 2 μL, dNTP (10 mmol L -1 ) 1.4 μL, Mg 2+ (25mmol·L -1 ) 1.4 μL, preamplified upstream primer and downstream primer (2 μmol L -1 ) each 2 μL, template DNA 3 μL 10ng / μL DNA, Taq DNA polymerase (5U·μL -1 , TaKaRa) 0.2μL, the balance is...
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