Quick clavibacter michiganensis subsp. michiganensis IMS-PCR (Polymerase Chain Reaction) detection kit, preparation method and use method thereof
A detection kit and tomato ulcer technology, applied in biochemical equipment and methods, DNA preparation, bacteria, etc., can solve the problems of long detection cycle, poor specificity, low sensitivity, etc., achieve short detection cycle, strong specificity, The effect of increasing the quarantine level
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Embodiment 1
[0046] Example 1: A rapid IMS-PCR detection kit for tomato canker pathogen, including 1 tube of 10×PCRBuffer, 1 tube of 2.5mM dNTPs, 1 tube of 5U Taq DNA polymerase, and 5μM upstream primer 5′-TCATTGGTCAATTCTGTCTCCC-3′200μL , 5μM downstream primer 5′-TACTGAGATGTTTCACTTCCCC-3′200μL, 1 tube of deionized water, 1 tube of PBST lotion, 1 tube of tomato ulcer pathogen specific immunomagnetic beads, 1 ordinary magnet with a volume of 2mm×3mm×5mm, positive Control 1 tube.
Embodiment 2
[0047] Example 2: See figure 2 , A method of using a rapid IMS-PCR detection kit for tomato canker pathogen, its main features are:
[0048] (1) Enrichment of pathogens: take 1 mL of the test sample and place it in a centrifuge tube, and then add 50 μL of tomato canker pathogen specific immunomagnetic beads into each centrifuge tube, the amount of magnetic beads is 10 5 -10 6 Pieces / mL, shake at room temperature for 2h on a shaker at a speed of 150rpm, then place the test sample on the magnet and let it stand for 5min. When the magnetic beads are collected on the side of the tube wall, carefully suck off the test sample with a pipette. Then wash the centrifuge tube 3 times with PBST for 2 minutes each time, let it stand on the magnet for 5 minutes, and then discard the washing solution;
[0049] (2) PCR amplification: resuspend the immunomagnetic beads enriched with pathogens in 50μL of deionized water, centrifuge and mix well, then transfer to the PCR tube, then put it in the PCR ...
Embodiment 3
[0051] Example 3: A method for preparing specific immunomagnetic beads of a rapid IMS-PCR detection kit for tomato canker pathogen, the main feature of which is that the steps are:
[0052] (1) Dissolve N-hydroxysuccinimide biotin (NHS-Biotin) in dimethylformamide (DMF) and adjust the biotin concentration to 50μg / mL;
[0053] (2) Determine the concentration of the antibody, and dilute the antibody to 10 μg / mL with a carbonate buffer of pH 9.6;
[0054] (3) Mix according to the mass ratio of biotin and antibody at a ratio of 1:10, and shake and react at room temperature for 4 hours;
[0055] (4) Cut the dialysis membrane with a molecular weight of 8000-14000 into small sections with a length of 5-10cm, and then add 500mL 2% NaHCO 3 And 1mmol / L Na with pH 8.0 2 EDTA·2H 2 Boil the dialysis membrane in O for 10 minutes, then thoroughly clean the dialysis membrane with deionized water, and then place it in 1mmol / L Na 2 EDTA·2H 2 Boil it in O for 10 minutes, cool it, and place it in a refrig...
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