Pulmonary tuberculosis variation activity marker, kit, method and model construction method
A pulmonary tuberculosis and active technology, applied in the field of biomedicine, can solve the problems of low sensitivity and poor specificity, and achieve the effect of overcoming low detection rate, good specificity and good clinical application value.
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[0055] The present invention will be further described below in conjunction with specific examples, but the examples do not limit the present invention in any form. Unless otherwise specified, the reagents, methods and equipment used in the present invention are conventional reagents, methods and equipment in the technical field.
[0056] Unless otherwise specified, the reagents and materials used in the following examples are commercially available.
Embodiment 1
[0058] Isolation of plasma samples from whole blood
[0059] The fasting peripheral blood of patients with active pulmonary tuberculosis was collected in the morning with EDTA anticoagulant tubes, centrifuged at 3000 rcf for 15 min, and the plasma was separated into a new 1.5 mL centrifuge tube within 6 hours. Plasma samples were stored in a -80°C freezer.
Embodiment 2
[0061] Determination of Protein Expression Level in Plasma Samples by ELISA
[0062] Plasma sample collection: 88 cases of active tuberculosis patients, 88 cases of healthy controls, and 88 cases of non-tuberculosis pulmonary respiratory diseases.
[0063] The expression levels of plasma protein markers were detected using human C1QB and CCL19 (MIP3B) kits (CLOUD-CLONE CORP.Whan.CN) according to standard operations. The t test or one-way ANOVA in GraphPad Prism 8 software was used for statistical analysis (when Pfigure 1 shown.
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