A detection kit for s100 protein
A technology for detecting kits and proteins, which is applied in the field of medical testing, can solve problems such as insufficient linear range, and achieve the effects of shortening detection time, high sensitivity and specificity, and improving sensitivity
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preparation example Construction
[0062] The preparation method of kit of the present invention is:
[0063] 1. Preparation of calibrator: Dissolve the S100 antigen in the diluent of the calibrator according to a certain concentration, and prepare the concentrations as 0ng / mL, 0.5ng / mL, 2ng / mL, 10ng / mL, 50ng / mL, 200ng / mL mL of calibrator solution, respectively recorded as S0, S1, S2, S3, S4, S5.
[0064] 2. Preparation of magnetic particle suspension: select the appropriate magnetic particle stock solution, coat the S100 antibody on the surface of the magnetic particle at a concentration of 0.1-1.0 μg / T, and prepare the S100 suspension for use.
[0065] 3. Prepare sample dilution: add 0.1% to 10% (w / v) chelating agent, 1‰ (w / v) preservative, 2% (w / v) to the Bis-Tris buffer system with pH 7.4 Protein stabilizer, 1‰ (w / v) dispersant, 1‰ (w / v) surfactant and 10-300μg / mL blocking agent were prepared as sample diluent.
[0066] 4. Preparation of enzyme conjugates: Add 1‰ (w / v) preservative, 1‰ (w / v) surfactant an...
Embodiment 1
[0072] Example 1 Preparation of S100 protein detection kit for melanoma diagnosis
[0073] 1. Kit preparation
[0074] 1. Prepare blocking solution
[0075] The blocking solution is prepared from 0.1M Tris buffer with pH 7.2, which contains 1‰ (w / v) preservative Proclin150, 2% (w / v) protein stabilizer hormone-free human serum, 1 % (w / v) of sucrose and 5% (w / v) of glycerol.
[0076] 2. Prepare enzyme conjugate dilution
[0077] Enzyme conjugate diluent is prepared by 0.05M pH 7.4 Bis-Tris buffer, which contains 1‰ (w / v) preservative Proclin150, 1‰ (w / v) surfactant Tween 20, 2% (w / v) protein stabilizer dehormone human serum and 0.5‰ (w / v) inert carmine pigment.
[0078] 3. Prepare sample diluent
[0079] The sample diluent is prepared by 0.05M pH 7.4 Bis-Tris buffer, which contains 5% (w / v) chelating agent EGTA, 1‰ (w / v) preservative Proclin150, 2% (w / v) / v) protein stabilizer dehormone human serum, 1‰ (w / v) dispersant sodium dodecyl sulfonate, 1‰ (w / v) surfactant Tween 20...
Embodiment 2
[0098] Embodiment 2 Test kit precision of the present invention
[0099] Three batches of kits were taken for precision experiments, and Q1, Q2, and Q3 were measured 20 times to calculate the variation in concentration. The results of the intra-analysis precision and inter-batch precision of the kits are shown in Table 1 and Table 2.
[0100] Table 1 Intra-analytical precision of kits
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[0103] Table 2 Precision between batches of kits
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[0106] It can be seen from the data in Table 1 that the coefficients of variation within the analysis of the three batches of low, medium and high concentration quality control products of the three batches of kits are all less than 6%. The batch-to-batch variation of control products is all less than 5%, indicating that the precision of the kit of the present invention is better.
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