Application of dermatopontin in preparing kit for detecting cardiac failure and detection kit
A heart failure and kit technology, which is applied to the application field of skin pontin in the preparation of heart failure detection kits, can solve the problems of low detection efficiency and difficult to obtain heart failure, and achieves low cost, high serum dilution ratio and high efficiency. high effect
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Embodiment 1D
[0038] Embodiment 1DPT and heart failure relation experiment
[0039] The etiology of arrhythmogenic right ventricular 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 chip and real-time PCR analysis, and the rest were fixed in 10% formalin for pathological examination and immunohistochemical analysis.
[0040] 1. Specific steps:
[0041] 1) Gene chip: use the gene chip to detect the genes differentially expressed in the myocardial tissues of ARVC patients...
Embodiment 2
[0051] Embodiment 2 uses kit of the present invention to detect the expression of serum DPT in end-stage heart failure group and normal group
[0052] Ninety-six cases of end-stage heart failure and 100 healthy controls were used to detect the expression of serum DPT in end-stage heart failure group and normal group, and the sensitivity and specificity of DPT in detecting heart failure were analyzed by ROC curve of SPSS17.0 software.
[0053] 1. Specific steps: DPT was assessed by enzyme-linked immunosorbent assay. According to the commercial DPT ELISA kit (product catalog) instructions. 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 solution was used for each ex...
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