Method for detecting glycated serum albumin by using boric acid affinity principle
A serum albumin and glycosylation technology, applied in the field of glycosylated serum albumin detection, can solve the problems of poor stability of enzyme and antibody protein, complicated steps, time-consuming, etc., and achieve the effect of stable reagents and rapid detection
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Embodiment 1
[0037] refer to Figure 1-2 , a method for detecting glycosylated serum albumin using the principle of boric acid affinity, characterized in that it comprises the following steps:
[0038] S1, get a certain volume of bromocresol violet solution in a cuvette;
[0039] S2, adding the serum sample to be tested into the bromocresol violet solution;
[0040] S3, obtain the total protein concentration C by measuring the absorbance at 585nm T ;
[0041] S4, adding the phenylboronic acid adsorbent to the cuvette to react with BCP-GA;
[0042] S5, waiting for the adsorbent to be completely deposited on the bottom of the cuvette;
[0043] S6, measure the absorbance at 585nm to obtain the concentration C of non-glycated albumin ng , and through the formula (C T -C ng ) / C T *100% is calculated as a percentage of serum albumin.
[0044] Wherein, steps S1, S2 and S3 are to obtain the absorbance A0 of the bromocresol violet solution at 585 nm under alkaline conditions, that is, the ...
Embodiment 2
[0061] The difference with Example 1 is:
[0062] The repetition rate of the method
[0063] Intra-batch repeatability test: Take the same serum sample and repeat the test 20 times continuously, and calculate the CV value. Batch-to-batch repeatability test: divide the same serum sample into 20 parts, store in the refrigerator, take 1 part for testing every day, for a total of 20 days, and calculate the CV value. The intra-assay CV value and the inter-assay (day) CV value should be less than 5% according to the requirements of the National Committee for Clinical Laboratory Standardization (NCCLS) documents, and the method meets the requirements.
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