Related Experiment Video
Updated: Sep 27, 2026

A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
[Establishment of a method for detecting anti-HCV IgM using recombinated structural region antigens]
Presence of IgM antibody to viral structural protein can be taken as the marker of its replication, so the detection method for anti-HCV IgM was established using as HCV recombinated structural region antigens, including C, E1, E2, as the coated antigen and rabbit anti-human gamma chain sera for neutralization and sheep anti-rabbit IgG coated for the sorbence of the complex of RAH-gamma with human IgG. 76 serum specimens of the hepatitis C patients were detected by indirect ELISA for anti-HCV IgM and by RT-PCR for RNA. The results suggested that IgM antibodies to C, E1, E2 were closely related with RNA (P < 0.005). The components of the IgM antibody, too were identified by indirect ELISA with recombined antigens coated respectively. When whole-fragment C or C + E2 were used as the coated antigens, anti-HCV IgM in 96.6% or 100% of serum specimens can be respectively detected. Using recombined structural region antigens, detection of anti-HCV IgM by ELISA was high sensitivity and specificity.
Presence of IgM antibody to viral structural protein can be taken as the marker of its replication, so the detection method for anti-HCV IgM was established using as HCV recombinated structural region antigens, including C, E1, E2, as the coated antigen and rabbit anti-human gamma chain sera for neutralization and sheep anti-rabbit IgG coated for the sorbence of the complex of RAH-gamma with human IgG. 76 serum specimens of the hepatitis C patients were detected by indirect ELISA for anti-HCV IgM and by RT-PCR for RNA. The results suggested that IgM antibodies to C, E1, E2 were closely related with RNA (P < 0.005). The components of the IgM antibody, too were identified by indirect ELISA with recombined antigens coated respectively. When whole-fragment C or C + E2 were used as the coated antigens, anti-HCV IgM in 96.6% or 100% of serum specimens can be respectively detected. Using recombined structural region antigens, detection of anti-HCV IgM by ELISA was high sensitivity and specificity.

