Probe capable of specifically identifying bisphenol A nucleic acid aptamer and test strip detection application of probe
A nucleic acid aptamer and test strip technology, which is applied in measuring devices, recombinant DNA technology, DNA/RNA fragments, etc., can solve problems such as inability to use on-site detection, limit widespread use, and high detection cost, and achieve application Broad range, high specificity, low cost effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0030] One aspect of the present invention also provides a method for preparing a bisphenol A immunochromatographic gold standard test strip, comprising:
[0031] Colloidal gold is reacted with the nucleic acid aptamer probe in the solution to form a nucleic acid aptamer probe-gold nanoparticle complex, and then the nucleic acid aptamer probe-gold nanoparticle complex is applied to the binding On the pad substrate, a nucleic acid aptamer probe-gold label binding pad is formed;
[0032] And, the bisphenol A-bovine serum albumin conjugate solution and the nucleotide chain solution capable of complementary pairing with the nucleic acid aptamer probe are respectively applied to the coated membrane substrate to form a detection line and a reference line independent of each other, Obtain the coating film;
[0033] And, at least the sample membrane, the nucleic acid aptamer probe-gold label binding pad, the coating film and the water-absorbing film are bonded to the liner in sequenc...
Embodiment 1
[0049]The specific operation steps of the preparation method of a bisphenol A immunochromatographic gold standard test strip based on nucleic acid aptamer probes involved in this embodiment are as follows:
[0050] (1) Select a 25-40nm colloidal gold solution, centrifuge at a centrifugal speed of 9500r / min for 7 minutes, discard the supernatant to obtain a 10-fold concentrated colloidal gold solution A;
[0051] Add 9 μL of 1 μM / L nucleic acid aptamer probe (abbreviated as ssDNA below) to 1 μL of acetate buffer solution and 1.5 μL of 1 μM / L TCEP for 1 h in the dark to obtain mixed solution B;
[0052] Add 100 μL of 10-fold concentrated colloidal gold solution A (concentration about 100 mM) to the above mixture B, and shake at room temperature for 30 minutes; add 85 μL of 100 μM / L dATP to the above solution, and shake at room temperature for 15 minutes; the shaking is completed Then add 20 μL of 0.1 M / L NaCl solution, let stand at room temperature for 30 min, and then put it in...
PUM
Property | Measurement | Unit |
---|---|---|
Length | aaaaa | aaaaa |
Particle size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com