Reagent plate for automatic pretreatment of nucleic acid detection
A reagent plate and nucleic acid sequencing technology, applied in the direction of biomass post-treatment, biomass pre-treatment, bioreactor/fermenter for specific purposes, etc., can solve the problems of unattended, sample impact, etc., to eliminate samples Effects of confusion, avoiding tediousness, and speeding up testing
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[0040] Example 1
[0041] like figure 1 The shown nucleic acid detection preprocessing automation device is composed of a moving rail platform 1 , a base 2 , a movable magnet 3 , a pipetting pump 4 and a pipetting tip 5 . The pipette tip 5 is arranged on the pipette pump 4, and the pipette pump can move along the moving rail platform 1 and rotate through the rotating module. The mobile rail platform 1 moves and rotates on the upper part of the reagent tray through the pipette pump and the pipette tip to realize pipetting. The base 2 has a temperature control module corresponding to the position of the reagent tray. Base 2 fits the reagent tray to provide temperature control. The reagent tray can be rotated and moved through the rotation module on the base 2 .
[0042] like Figure 2-3 The reagent tray shown includes a cover plate 6 and a reagent tray 7. The reagent tray 7 is provided with several reagent holes 8. The reagent holes 8 are filled with nucleic acid sequencing...
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[0044] Example 2
[0045] Plasma cell-free DNA is small fragment and fragmented DNA, the fragment length is between 100 and 300 bp, and the peak value is about 160 bp. In 1997, Professor Lu Yuming discovered that fetal cell-free DNA was contained in the peripheral plasma of pregnant women, thus pioneering the use of cell-free DNA as the source of detection to analyze whether the fetus carried by pregnant women had chromosomal abnormalities. Circulating tumor DNA (ctDNA) derived from tumor cells also exists in plasma. ctDNA is widely used for tumor liquid biopsy, which can be used for non-invasive early diagnosis, companion diagnosis, and prognosis follow-up.
[0046] The conventional detection method is to first extract DNA from clinical samples including plasma, and then perform three steps of nucleic acid detection processing and detection. It takes 6 to 13 hours to complete the entire sample test. Among them, sample nucleic acid extraction and pre-detection processing are...
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[0063] Example 3
[0064] The research object of transcriptome sequencing is the sum of all RNAs that can be transcribed by a specific cell in a functional state, mainly including mRNA and non-coding RNA. Transcriptome research is the basis and starting point of gene function and structure research. Through next-generation high-throughput sequencing, almost all transcript sequence information of a specific tissue or organ of a species can be obtained comprehensively and quickly in a certain state, which has been widely used. In basic research, clinical diagnosis and drug development and other fields.
[0065] The conventional detection method is to first extract RNA from clinical samples including whole blood and plasma, and carry out three steps of nucleic acid detection processing and detection. It takes 6 to 30 hours to complete the entire sample test. Among them, sample nucleic acid extraction and pre-detection processing are cumbersome.
[0066] The nucleic acid detect...
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