Colloid selenium test paper for semi-quantitative determination of urinary trace albumin
A technology for semi-quantitative detection of urine microalbumin, applied in the field of in vitro disease detection instruments and equipment, semi-quantitative detection of urine microalbumin colloidal selenium test paper, can solve the problems of unsuitability for on-site detection, long RIA determination process, expensive instruments, etc. Achieve the effect of convenient home testing and on-site testing, real-time monitoring and tracking, and accurate and reliable results
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Embodiment 1
[0019] Example 1 Preparation of urinary microalbumin monoclonal antibody
[0020] Mice were immunized with human serum albumin (product of Sigma, USA). The mouse splenocytes whose titer reaches the requirement are selected for hybrid fusion with mouse myeloma cells to prepare hybridoma cells. Select high positive hybridoma cells for multiple subcloning until a cell line that can stably secrete MAU monoclonal antibody is selected.
[0021] Ascites was induced by inoculating hybridoma cells into the peritoneal cavity of mice, and the ascites was extracted and purified to obtain monoclonal antibodies 1 and 2, which proved to target different epitopes on the antigen.
Embodiment 2
[0022] The preparation of embodiment two colloidal selenium
[0023] Add 10% chitosan to the reactor, add ascorbic acid, selenous acid, and ascorbic acid in turn after 2 minutes, and add selenous acid and ascorbic acid at intervals from the fourth minute of the reaction, and then scan the spectrum, and the peaks appear at 500-600nm The maximum absorption peak is appropriate, and the product is collected for future use.
Embodiment 3
[0024] Example 3 Preparation and assembly of colloidal gold test paper for semi-quantitative detection of MAU
[0025] 1. Treatment of the sample liquid absorption part:
[0026] Soak the filter paper or glass fiber paper in 0.1mol / l PBS with pH7.4 for 2min, take it out, dry it at 80°C or dry it by other methods, and then it becomes the absorption part of the sample solution.
[0027] 2. Preparation and processing of colloidal selenium-labeled fractions:
[0028] Mix colloidal selenium and MAU monoclonal antibody 1 in a certain ratio to form MAU monoclonal antibody 1 He Li Tan Qiao Xiao
[0029] 2.1 Pretreatment of MAU monoclonal antibody 1 to be labeled
[0030] Pre-dialyze MAU monoclonal antibody 1 in 0.005mol / l NaCl, pH7.0 solution at 4°C overnight to remove excess electrolyte, then centrifuge at 6500-13000r / min at 4°C for 60min to remove the precipitate, adjust the protein concentration to 1mg / ml and then use it to mark.
[0031] Optimize the experimental conditions ...
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