Antigen mimotope ph1 of bisphenol A and its application
A technology that mimics epitopes and antigens. It is applied in the direction of recombinant DNA technology, DNA/RNA fragments, and material inspection products. It can solve the problems of restricting the application and promotion of immunological methods, easily causing harm to testing personnel and the environment, and increasing testing costs. , to achieve cost saving, good effect, and reduce the harm to human health
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Embodiment 1
[0017] Example 1. Affinity panning and identification of bisphenol A antigen mimotope
[0018] Affinity panning of mimotopes of bisphenol A antigen: the specific method is: dilute anti-bisphenol A monoclonal antibody with 10mMPBS (pH7.4), and coat a 96-well microtiter plate with a final concentration of 75μg / mL, at 4°C Incubate overnight. The next day, wash 10 times with TBST (50mM NaCl, pH7.5 containing 0.1% Tween-20 (v / v)), add 300μL blocking solution (3%BSA-PBS) and incubate at 4°C for 2 hours. Discard the blocking solution after two hours, and dilute the phage stock solution 10 times with TBS, about 1.0×10 11 pfu). Shaking reaction at 25°C for 2 hours. Unbound phages were discarded, washed 10 times with TBST, bound phages were eluted with 0.2MGlycine-HCl (pH2.2), and immediately neutralized with 15μL 1M Tris-HCl (pH9.1). Take 10 μL of the eluted phage to measure the titer, and the rest is used to infect 20 mL of the E.ColiER2738 strain grown to the pre-logarithmic stag...
Embodiment example 2
[0022] Implementation Case 2. Sequencing of the Bisphenol A Antigen Mimotope Encoding Gene and Determination of its Amino Acid Sequence
[0023] The phages displaying bisphenol A antigen mimic epitopes identified by indirect competition ELISA in Example 1 were amplified, and the DNA sequencing templates of the phages were extracted. The brief process is as follows: carry out phage amplification, and transfer 800 μL of phage-containing supernatant into a new centrifuge tube after the first centrifugation. Add 200 μL PEG / NaCl to precipitate the phage. After centrifugation, resuspend the pellet in 100 μL of iodide buffer (10 mM Tris-HCl (pH 8.0), 1 mM EDTA, 4M NaCl), add 250 μL of absolute ethanol to precipitate DNA, and wash the pellet (DNA sequencing template) with 70% ethanol after centrifugation. The pellet was finally resuspended in 20 μL of sterilized water, and 2 μL was taken for agarose gel electrophoresis analysis; 5 μL of phage template was taken for DNA sequencing, an...
Embodiment example 3
[0024] Implementation Case 3 Application of Bisphenol A Antigen Mimotope as Competing Antigen in ELISA
[0025] (1) Sample extraction
[0026] Weigh 5g of sample (cereals and related foods), add 25ml of 60% methanol-PBS solution, shake at 200rpm for 5min; filter the extract with whatman No. 1 filter paper, take 1ml of the filtrate and add 4ml of PBS (phosphate buffered saline solution, pH = 7.2) after mixing, it is the sample extraction solution, ready for use.
[0027] (2) Coating and sealing
[0028] Dilute the anti-bisphenol A monoclonal antibody with 10mMPBS (pH7.4), coat the microtiter plate with 10μg / mL, and incubate overnight at 4°C. The next day, after washing 3 times with PBST (10mMPBS, 0.05% Tween-20 (v / v)), block with PBS containing 3% skimmed milk powder, incubate at 37°C for 1 hour, wash the plate 6 times with PBST for use .
[0029] (3) Establishment of standard curve
[0030] Take out the plates that have been treated in step (2), and put 50 μL of phage (1.0×...
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