Application of LTBP-2 (Latent transforming growth factor beta binding protein 2) in preparation of cardiac failure test kit and kit containing LTBP-2
A 1. LTBP-2, heart failure technology, applied in biological testing, material testing products, etc., can solve the problems of neglect of heart failure, single marker or multiple markers of heart failure, etc., to achieve high serum dilution ratio and cost. Low, easy-to-use effects
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Embodiment 1
[0041] Example 1: Experiment on the relationship between LTBP-2 and heart failure
[0042] The etiology of right ventricular arrhythmogenic heart disease (ARVC) is still unclear, and the main feature is that the right ventricular myocardium is replaced by fibrofatty tissue, causing repeated ventricular arrhythmias. Our 5 heart failure patients with ARVC mainly showed left ventricular dysfunction, and the pathology confirmed that the left ventricular free wall was replaced by fibrofatty tissue. Each specimen was obtained from the left ventricular free wall of a failing heart after heart transplantation and a non-failing donor heart. Some specimens were immediately frozen and stored in liquid nitrogen for gene chips and real-time PCR, and the rest were fixed in 10% formalin for pathological examination.
[0043] Specific steps:
[0044] 1) Gene chip: Use the 70-mer oligonucleotide chip of CapitalBio to detect multiple genes in the myocardial tissues of ARVC heart failure patie...
Embodiment 2
[0054] Embodiment 2 detects the expression of serum LTBP-2 of end-stage heart failure group and normal group with LTBP-2 kit
[0055] There were 96 cases of end-stage heart failure and 100 cases of healthy controls. The expression of serum LTBP-2 in the end-stage heart failure group was significantly higher than that in the control group, P<0.01, and there was a significant statistical difference.
[0056] ELISA specific procedure: LTBP-2 was assessed by enzyme-linked immunosorbent assay. According to the instructions of the ELISA kit of LTBP-2 (product catalog No. ESBL2196, Ever systems Biology Laboratory Inc.). Set blank wells, standard wells and sample wells to be tested respectively. Add 100 μl of sample diluent to the blank well, add 100 μl of standard substance or test sample to the remaining wells, shake gently to mix, cover or cover the microtiter plate, and react at 37°C for 120 minutes. In order to ensure the validity of the experimental results, a new standard sol...
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