An internal standard-based RT‑PCR detection technique for apple rust viroids
A rust fruit-like virus, RT-PCR technology, applied in the direction of microorganism-based methods, microorganism measurement/inspection, microorganisms, etc., can solve the problems of prone to false negative phenomena, low content, uneven distribution, etc., to avoid false negatives Results, good detection stability, and the effect of reducing loss
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[0009] Take the top 0-5 cm cortex tissue of the annual branch of apple with leaf buds as the test material, take 100 mg tissue, grind it rapidly in liquid nitrogen, add 0.5 mL extraction reagent (400 μL RNA extraction reagent + 100 μL β-mercaptoethanol) for extraction , and finally add 20 μL DEPC water to fully dissolve the RNA. Then, using specific primers ASSVdQCxin and nad 5 as primers, M-MLV reverse transcriptase was used to synthesize cDNA, and the synthesized cDNA was used as a template to prepare the following PCR reaction system: cDNA template 3.0 μL, ASSVdQCxin-3' (20 pmol / μL ) 1 μL, ASSVdQCxin-5' (20 pmol / µL) 1 μL, nad 5 -3' (20pmol / µL) 0.1 µL, nad 5 -5' (20 pmol / µL) 0.1 μL, 2×ES Taq Mastermix 12.5 μL, with ddH 2 Make up 25 μL with O; PCR program: pre-denaturation at 94°C for 3 min; 35 cycles: denaturation at 94°C for 1 min, annealing at 61.0°C for 45 s, extension at 72°C for 30 s; final extension at 72°C for 10 min; take 5 μL of PCR amplification Amplified produc...
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