Viral Antigens
Product List
HCV Core 22kDa, FLSCN
Hepatitis C Virus Core 22kDa, FLSCN Recombinant
The E.coli derived recombinant protein contains the HCV core nucleocapsid immunodominant regions, amino acids 2-192. The FLSCN labeled protein is fused with b-galactosidase (114 kDa) at N-terminus.
HCV Core 22kDa, Rhodamine
Hepatitis C Virus Core 22kDa, Rhodamine Recombinant
HCV Core 24
Hepatitis C Virus Core 24 Recombinant
HCV Core Genotype-1
Hepatitis C Virus Core Genotype-1 Recombinant
HCV Core Genotype-1a
Hepatitis C Virus Core Genotype-1a Recombinant
HCV Core Genotype-1b
Hepatitis C Virus Core Genotype-1b Recombinant
HCV Core Genotype-1b Biotin
Hepatitis C Virus Core, Biotin Recombinant
The E.coli derived recombinant Biotin Labeled protein contains the HCV core nucleocapsid immunodominant regions, amino acids 2-119, having an MW of 22kDa. The protein is fused to a beta-galactosidase (114 kDa) at the N-terminus.
HCV Core Genotype-2a
Hepatitis C Virus Core Genotype-2a Recombinant
HCV Core Genotype-2b
Hepatitis C Virus Core Genotype-2b Recombinant
The E.coli derived recombinant protein contains the HCV core nucleocapsid immunodominant regions, amino acids 2-119.
The protein is fused to a GST tag at N-Terminus.
HCV Core Genotype-3/10
Hepatitis C Virus Core Genotype-3/10 Recombinant
Introduction
Hepatitis C is a liver disease caused by the hepatitis C virus (HCV), a small, enveloped, positive-sense single-stranded RNA virus belonging to the genus Hepacivirus within the family Flaviviridae . HCV can cause both acute and chronic hepatitis, ranging from a mild illness lasting a few weeks to a serious, lifelong illness including liver cirrhosis and cancer . There are seven major genotypes and numerous subtypes of HCV, which vary in their geographical distribution and response to treatment .
HCV particles are spherical and range from 40 to 80 nanometers in diameter . The virus has a lipid membrane envelope embedded with two glycoproteins, E1 and E2, which play crucial roles in viral attachment and entry into host cells . HCV primarily infects hepatocytes in the liver but can also be found in other tissues such as lymph nodes and peripheral blood mononuclear cells . The virus exhibits significant genetic diversity, which contributes to its ability to evade the host immune system .
HCV’s primary function is to replicate within host cells. It hijacks the host’s cellular machinery to produce viral proteins and RNA . The virus plays a role in immune evasion by interfering with the host’s immune responses, including the inhibition of interferon signaling pathways . HCV also induces chronic inflammation, which can lead to liver fibrosis, cirrhosis, and hepatocellular carcinoma .
HCV enters host cells through interactions with several receptors, including the low-density lipoprotein receptor (LDLr), heparan sulfate proteoglycans (HSPGs), scavenger receptor B1 (SRB1), and CD81 . Once inside the cell, the virus releases its RNA genome, which is translated into a single polyprotein. This polyprotein is then cleaved into structural and non-structural proteins that are essential for viral replication . The virus also manipulates host cell signaling pathways to create a favorable environment for its replication .
The expression and activity of HCV are regulated at multiple levels. Transcriptional regulation involves the interaction of viral RNA with host cell factors that enhance or inhibit viral replication . Post-translational modifications, such as phosphorylation and ubiquitination, also play critical roles in regulating the stability and function of viral proteins . Additionally, HCV can modulate host immune responses to promote viral persistence .
HCV research has led to significant advancements in understanding viral pathogenesis and developing therapeutic strategies. Direct-acting antivirals (DAAs) have revolutionized HCV treatment, offering high cure rates with fewer side effects compared to previous therapies . HCV is also used as a model to study RNA virus replication and host-virus interactions . Diagnostic tools, such as serological assays and nucleic acid tests, are essential for detecting HCV infection and monitoring treatment response .
HCV’s life cycle begins with the attachment of the virus to host cell receptors, followed by entry into the cell via endocytosis . Once inside, the viral RNA is released and translated into a polyprotein, which is processed into functional viral proteins . These proteins facilitate viral RNA replication and assembly of new virions, which are then released to infect other cells . Throughout its life cycle, HCV interacts with various host factors to ensure its replication and persistence .
