Composition for detecting immune antibodies of rheumatoid arthritis by dot immunogold filtration assay
A technology of immune diafiltration and immune antibody, which is applied in biological testing, measuring devices, material inspection products, etc., can solve the problems of no data supporting BiP rheumatoid arthritis, waiting for further independent clinical research, and the impact of detection sensitivity
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Embodiment 1
[0096] The synthesis of embodiment 1CCP peptide I and CCP peptide II
[0097] CCP peptides can be synthesized by solid-phase synthesis techniques using Fmoc chemistry. For the specific steps of this method, see Eur.J.Immunol.1994, 24, 3188-3193; J.Org.Chem.1972, 37, 3404-3409; Huang Weide, Chen Changqing Polypeptide Synthesis, Beijing: Science Press, 1985.
[0098] The formation method and steps of disulfide bonds can be found in the literature: Huang Weide, Chen Changqing Peptide Synthesis, Beijing: Science Press, 1985, p85; Michael W.Pennington Peptide Synthesis Protocols (Methods in Molecular Biology), Humana Press, 1994, p91- 169.
[0099] In this example, various CCP peptides were synthesized by Jill Biochemical (Shanghai) Co., Ltd., and the specific sequences are as follows:
[0100] CCP peptide I: His-Gln-Cys-His-Gln-Phe-Arg-Phe-Cit-Gly-Cit-Ser-Arg-Ala-Ala-Cys-Gly, on which the third and sixteenth Cys pass The sulfhydryl group forms a disulfide bond, and makes the po...
Embodiment 2
[0102] Example 2 The Combination of CCP Peptide I and CCP Peptide II with High Molecular Polymers
[0103] Dissolve 2 mg of carrier protein BSA in 200 μl of deionized water, 2 mg of CCP peptide I and CCP peptide II (molar ratio 1:1) in 0.5 ml of coupling buffer (0.1 mol / L MES, 0.9 mol / L NaCl, 0.2 g / L L NaN 3 , pH4.7). Add 0.5 ml of CCP solution to 200 μl of carrier protein solution. Add 1ml of 1-ethyl-(3-dimethylaminopropyl)carbodiimide (EDC) solution with a concentration of 10mg / ml into the mixture of CCP and BSA, mix gently, and react at room temperature for 2h , dialyzed with 0.01mol / L pH7.4 phosphate buffer at 4°C for 3 days, and stored at 4°C after aliquoting.
Embodiment 3I
[0104] Example 3 IgG labeled colloidal gold
[0105] Heat 99ml ultrapure water to 80-90°C, add 1% (w / v) HAuCl 4 1ml, continue heating and stirring until boiling. Fill and boil for about 10 seconds, quickly add the existing trisodium citrate solution (0.0236g trisodium citrate, made into a concentration of about 1% (w / v)), stir and boil for 10 minutes. After cooling at room temperature, add ultrapure water to make up to 100ml. Scan the obtained colloidal gold at a wavelength of 400-700nm, and require the absorption value at a wavelength of 525-535nm to reach 0.92-0.98.
[0106] In 100ml of prepared gold sol that has been cooled to room temperature, use 1% (w / v) K 2 CO 3 Adjust the pH to 8.2.
[0107] Add 1.5 mg mouse anti-human IgG (Hangzhou Keelong Biotechnology Co., Ltd.) (0.1 M phosphate buffer diluted to 1 mg / ml), and stir at room temperature for 30 min.
[0108] Add BSA solution to block for 30min (5% (w / v) solution, add 25ml). Centrifuge at 10,000rpm for 25min and ...
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