A detection kit and detection method for Fusarium wilt of cabbage
A technology of cabbage wilt pathogen and detection kit, which is applied in the direction of microbial measurement/inspection, biochemical equipment and methods, etc., can solve the problems of long cycle time, and achieve the effect of simple and fast operation, good practicability, and strong practicability
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Embodiment 1
[0032] Embodiment 1: the detection kit of Fusarium wilt of cabbage of the present invention, this kit comprises, the detection upstream primer Foc-R of concentration all is 10pmol / μl, downstream primer Foc-S each 1μl, 10×PCREasyTaq buffer solution 2.0μl, 0.5 μl of 10 mM dNTPs, 0.4 μl of Taq polymerase with an active enzyme concentration of 5 U / ml, 1 μl of Brassica wilt positive control DNA, and 20 ul of ultrapure water with a weight concentration ≥ 99%. Sequences of detection primers:
[0033] The sequence of Foc-R 5'-TCAATGATAGTGACAAGGGTTT-3',
[0034] Sequence of Foc-S 5'-AATTTGCTGTGATAGGTGGAT-3'
[0035] The method for using the kit of the present invention to detect Fusarium wilt of cabbage comprises the following steps, (1) utilizing the CTAB method to extract plant tissue DNA infected by Fusarium cabbage, or utilizing the PowerSoilDNAIsolationKit kit method to extract soil DNA infected by Fusarium cabbage ;
[0036] (2) Using a detection kit to perform PCR amplification...
Embodiment 2
[0048] Embodiment 2: Utilize the method of Embodiment 1 to detect Fusarium wilt in the diseased cabbage plant tissue.
[0049] 1. Sample collection: Plant tissue samples were collected from the cabbage vegetable base in Xiaoyingfang Village, Yanqing District, Beijing
[0050] 2. DNA extraction and detection: the same as in Example 1.
[0051] 3. Test result: the result is visible figure 2 , a clear specific band with a molecular weight of 436bp was seen, so it was judged that the diseased tissue was infected with Fusarium wilt.
Embodiment 3
[0052] Embodiment 3: Utilize the method of Embodiment 1 to detect the Fusarium wilt of cabbage in the soil sample.
[0053] 1. Sample collection: Soil samples were collected from the experimental greenhouse of the Vegetable and Flower Research Institute of the Chinese Academy of Agricultural Sciences.
[0054] 2. DNA extraction and detection:
[0055] Soil samples were extracted with the method described in the MOBIO PowerSoilDNAIsolationKit kit, and PCR amplification was carried out according to the method implemented in the above kit. The PCR reaction system was 20 μl, including 2.0 μl of 10×PCR reaction buffer, 0.5 μl of 10 mMdNTPs, and 5 U / μl of EasyTaq polymerase 0.4 μl, 1 μl of 10pmol / μl primers Foc-R / Foc-S, 1 μl of 5ng / μl DNA template, and 20 μl of ddH2O. The PCR amplification program is: 94°C 5min; 94°C 40sec; 63°C 30sec; 72°C 1min; 35cycles, 72°C 10min. Amplified products were detected by electrophoresis.
[0056] 3. Test results; see results image 3 , a clear sp...
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