Use of CD157 gene
A CD157-R, gene technology, applied in the field of bioengineering, can solve the problems of long time, high laboratory biosafety requirements, false positives, etc., and achieve the effect of accurate tuberculosis diagnosis
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Embodiment 1
[0024] In this embodiment, the population is divided into three groups: tuberculosis patients, latent infection population and healthy population (20 cases each). By detecting the change of CD157 gene mRNA in each peripheral blood mononuclear cell (PBMC), it is found that it is present in tuberculosis patients. A clear trend of up-regulated expression.
[0025] In this example, quantitative RT-PCR method was used to detect the expression changes of CD157 gene in each case. Specific steps are as follows:
[0026] Step 1: Preparation of Peripheral Blood Mononuclear Cell (PBMC) Suspension
[0027] Add 5ml of lymphocyte separation medium (Fresenius Kabi NOrgeAs: LYS3773) into the centrifuge tube; take 2ml of heparin anticoagulated venous blood from the above-mentioned confirmed tuberculosis patients, patients with latent infection and healthy people and an equivalent amount of 1M phosphate buffer solution (PBS) Mix well to obtain a mixed solution, use a pipette to slowly superi...
Embodiment 2
[0056] In this embodiment, the crowd is divided into three groups: 9 cases of tuberculosis patients, 6 cases of latently infected people and healthy people, and the changes of CD157 gene mRNA in each peripheral blood mononuclear cell (PBMC) were detected by gene chip, and it was found that it was significantly different in tuberculosis patients. There was a clear trend of up-regulated expression.
[0057] In this embodiment, the gene chip is used to detect the difference in gene expression level of CD157 gene in TB, LTBI, and HC in tuberculosis samples, including the following four steps:
[0058] Step 1: Chip Preparation
[0059] At present, glass or silicon wafers are mainly used as carriers to prepare chips, and target genes are arranged in sequence as probes on the carrier by spotting method. Target genes can be divided into genomic DNA and cDNA (or artificially synthesized DNA).
[0060] Step 2: Sample Preparation
[0061] The extraction steps of total RNA in the sample...
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