Self-suction type multichannel pathogenic bacterium detection micro-fluidic chip based on LAMP (loop-mediated isothermal amplification)
A pathogenic bacteria detection and microfluidic chip technology, applied in the field of microbial detection, can solve problems that have not yet been combined with multi-channel pathogenic bacteria detection microfluidic chips
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Embodiment 1
[0052] Example 1 Selection of SA and VP characteristic nucleic acid sequences and design and screening of corresponding LAMP primers
[0053] According to species specificity, SA's nuc 300bp conserved nucleic acid fragment and VP in the gene tlh The 400bp conserved nucleic acid fragment in the gene was selected as the respective characteristic sequence. 6 LAMP primers corresponding to the SA signature sequence (F3- nuc 、B3- nuc , LF- nuc , LB- nuc , FIP- nuc , BIP- nuc ) self-designed by using computer software; 6 primers corresponding to the VP characteristic sequence (F3- tlh 、B3- tlh , LF- tlh , LB- tlh , FIP- tlh , BIP- tlh ) was obtained based on literature review (Yamazaki, W., Ishibashi, M., Kawahara, R., Inoue, K., 2008. BMC Microbiol. 8, 163.). All primers were synthesized by Sangon Bioengineering (Shanghai) Co., Ltd. The characteristic sequences and primer sequences are shown in Table 1.
[0054] Table 1. List of characteristic sequences and pri...
Embodiment 2
[0056] Example 2 Preparation of LAMP-based self-priming multi-channel pathogen detection microfluidic chip
[0057] Three-dimensional schematic diagram of self-priming multi-channel pathogen detection microfluidic chip based on LAMP figure 1 As shown, the actual picture is as figure 2 As shown, the exploded diagram is as image 3 As shown, the chip includes a sampling layer 1, a reaction layer 2 and a support layer 3 from top to bottom; the sampling layer 1 includes a sampling port 4, a sampling channel 5 and a nanoscale anti-evaporation film 8; The reaction layer 2 includes a reaction chamber 6 and a circular filter paper sheet 7;
[0058] In the sampling layer 1, the sampling channel 5 is located at the bottom of the layer, one end converges at the sampling port 4, and the other end communicates with the reaction chamber 6; the sampling channel 5 has three channel walls in the sampling layer 1, and the bottom Hollow out; when the sampling layer 1 and the reaction layer ...
Embodiment 3
[0067] Example 3 SA plasmid template detection of self-priming multi-channel pathogen detection microfluidic chip based on LAMP
[0068] 1. Configuration of LAMP reaction solution
[0069] every 8 mu L LAMP reaction solution contains the following components: 0.8M betaine, 1.4 mM dNTP solution, 0.8 mu L 10 × Isothermal Amplification Buffer, 6 mM Magnesium Sulfate Solution, 0.16 mu L 10 × SYBR Green I fluorescent dye, 300 mu M Hydroxynaphthol Blue Solution, 2.56 U Bst 2.0 Hot Start DNA Polymerase, 430 copies / mu L Plasmid template containing SA signature sequence; if there are N reaction chambers on the chip, configure 8×N mu L reaction solution.
[0070] 2. Chip degassing
[0071] Use scotch tape to seal the injection port of the prepared chip; place the chip in a vacuum desiccator, and degas it under 10kPa pressure for 1 hour.
[0072] 3. Self-priming sample injection
[0073] Use a pipette to draw the LAMP reaction solution, and insert the tip with the react...
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