Real-time Fluorescence Quantitative PCR in Detecting CD_(58) Gene Expression in PBMC in Patients with HBV Infection
Xiangling Wang
Abstract
Xiangling Wang
Abstract
Objective To quantitatively detect the expression level of CD_(58) in PBMC in the patients with HBV infection. Methods The total RNA isolated from PBMC was reversely transcribed into cDNA. The real-time fluorescence quantitative PCR method was used to analyze the expression level of CD_(58) gene in all patients and normal controls. The serum levels of ALT and AST were detected meanwhile. Results The real-time fluorescence quantitative PCR method was performed successfully to precisely detect the mRNA level. The expression level of CD_(58) gene in patients with HBV infection was significantly higher than those in control. The level of CD_(58) mRNA in PBMC from patients with HBV infection were positively correlated with serum levels of ALT and AST. Conclusion The real-time fluorescence quantitative PCR is the most precise method to quantitatively detect the mRNA level and can be used in gene expression changes. The expression level of CD_(58) gene is related with the degree of HBV infection and the degree of liver damage.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To quantitatively detect the expression level of CD_(58) in PBMC in the patients with HBV infection. Methods The total RNA isolated from PBMC was reversely transcribed into cDNA. The real-time fluorescence quantitative PCR method was used to analyze the expression level of CD_(58) gene in all patients and normal controls. The serum levels of ALT and AST were detected meanwhile. Results The real-time fluorescence quantitative PCR method was performed successfully to precisely detect the mRNA level. The expression level of CD_(58) gene in patients with HBV infection was significantly higher than those in control. The level of CD_(58) mRNA in PBMC from patients with HBV infection were positively correlated with serum levels of ALT and AST. Conclusion The real-time fluorescence quantitative PCR is the most precise method to quantitatively detect the mRNA level and can be used in gene expression changes. The expression level of CD_(58) gene is related with the degree of HBV infection and the degree of liver damage.
Key concepts: Real-time polymerase chain reaction, Peripheral blood mononuclear cell, Medicine, Gene expression, Gene, Complementary DNA, Messenger RNA, Molecular biology