Kit and method for extracting nucleic acids from urine
A technology for extracting nucleic acid and extraction method, which is applied in the field of biology, can solve the problems of long sample loading time, loss of free nucleic acid, unfavorable nucleic acid extraction, etc., and achieves the effect of simple operation, high purity of nucleic acid, and saving operation time
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Embodiment 1
[0034] Take 10mL of fresh urine from a healthy person, add 15mL of lysate ULB, mix by inverting, and bathe in water at 37°C for 10 minutes. Assemble the suction filtration device to the suction filtration bottle to configure a complete suction filtration system (see figure 1 ). Pour the sample into the sample tube, start the air pump, and after the sample completely passes through the adsorption column, turn off the air pump and take out the adsorption column. Add 500 μL of LUWB1 to the adsorption column, centrifuge at 12000 rpm for 1 min, add 500 μL of LUWB2, centrifuge at 12000 rpm for 1 min, and finally use 35 μL of eluent for elution.
[0035] PCR amplification experiment: take human GAPDH as the target gene, take 2 μL of the eluted nucleic acid solution as a PCR template, add 11 μL of deionized water and 7 μL of premix, and the reaction system is 20 μL. The premix preparation method is shown in Table 5, and the PCR reaction program is shown in Table 6.
[0036] Primer ...
Embodiment 2
[0044] Take 20mL of urine from a patient diagnosed with pancreatic cancer, and do two parallel experiments, each tube of urine sample is 10mL. Add 15mL lysate solution ULB to each, invert and mix well, and bathe in water at 37°C for 10 minutes. Assemble the suction filtration device to the suction filtration bottle to configure a complete suction filtration system (see figure 1). Pour the sample into the sample tube, start the air pump, and after the sample completely passes through the adsorption column, turn off the air pump and take out the adsorption column. Add 500 μL of LUWB1 to the adsorption column, centrifuge at 12000 rpm for 1 min, add 500 μL of LUWB2, centrifuge at 12000 rpm for 1 min, and finally use 35 μL of eluent for elution.
[0045] PCR amplification experiment: take the human mutated KRAS as the target gene, take 2 μL of the eluted nucleic acid solution as a PCR template, add 11 μL of deionized water and 7 μL of the premix, the reaction system is 20 μL, and...
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