Soybean phytophthora testing reagent kit and its test method
A detection kit, Phytophthora soybean technology, applied in the biological field, can solve the problems of long cycle and low sensitivity, and achieve the effect of high accuracy and high sensitivity
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Embodiment 1
[0038] Detect Phytophthora soybean in the soil sample of embodiment 1
[0039] Phytophthora soybean detection kit, including the following components:
[0040] Specific primer sequences for Phytophthora sojae
[0041] Upstream (18bp): 5'CTGGATCATGAGCCCACT 3'(Pso1)
[0042] Downstream (16bp): 5'GCAGCCCGAAGGCCAC 3'(Pso2)
[0043] Kit reaction system
[0044] 1mL detection solution includes: 0.05mmol Tris.Cl, 0.125mmol KCl, 0.005mmol MgCl 2 , 0.01mmoldNTPs, upstream and downstream primers 0.25mmol, 0.1mgBSA, Taq DNA polymerase 100 units, add ultrapure water to prepare 1mL detection solution. The solution was stored in a -20°C freezer. The storage period is 1 year. Example 1 Detection of Phytophthora soybean from soil samples of imported soybeans with bacteria:
[0045] The method that the above-mentioned Phytophthora soybean detection kit is used to detect Phytophthora soybean includes:
[0046] 1) Enrichment of oospores in soil:
[0047] Take 20-100 grams of the soil sam...
example 2
[0059] Example 2 Detection of zoospores of Phytophthora sojae from polluted water
[0060] Take 500mL of irrigation water contaminated by Phytophthora sojae, centrifuge it for 20min under the centrifugal force of 6000g, discard the supernatant, suspend the precipitated zoospores with 100uL water, transfer them into a 1.5mL centrifuge tube, add 0.05g of quartz sand, and vortex For 10 sec, take 1uL of the zoospore fragmentation solution as a template to obtain 100% specific amplification products. Wherein, 2-3 μl template PCR template is used for gene amplification according to the method of Example 1, and a unique fragment of Phytophthora sojae can be amplified. figure 2
[0061] Note: When using this method for detection, it should be noted that it is best to crush the sample before loading, and the crushed solution should not be placed for a long time. The detection sensitivity of this method is 0.1-1 zoospore per milliliter of polluted water.
example 3
[0062] Example 3 Identification of Phytophthora sojae from diseased soybean tissues
[0063] After sterilizing the soybean leaves or rhizome parts with water-soaked lesions with 70% alcohol, extract DNA by CTAB method or alkali lysis method, draw 1uL DNA solution, carry out PCR amplification according to the method of Example 1, and electrophoresis detection amplification If the product is a disease caused by Phytophthora soybean infection, a clear specific band with a molecular weight of 330bp can be seen, and the results are shown in image 3 .
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