HAVCR1 Mouse

Hepatitis A Virus Cellular Receptor 1 Mouse Recombinant

HAVCR1 produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 222 amino acids (22-237 a.a.) and having a molecular mass of 24.4kDa (Migrates at 40-57kDa on SDS-PAGE under reducing conditions). 
HAVCR1 is expressed with a 6 amino acid His tag at C-Terminus and purified by proprietary chromatographic techniques.
Shipped with Ice Packs
Cat. No.
BT9138
Source
Sf9, Baculovirus cells.
Appearance
Sterile Filtered colorless solution.

HAVCR2 Human

Hepatitis A Virus Cellular Receptor 2 Human Recombinant

Recombinant Human HAVCR2 produced in E. coli is a single polypeptide chain containing 206 amino acids (aa 22-202) and having a molecular mass of 22.7kDa.
HAVCR2 is fused to a 25 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.
Shipped with Ice Packs
Cat. No.
BT9327
Source
Escherichia Coli.
Appearance
Sterile filtered colorless solution.

HAVCR2 Human, Sf9

Hepatitis A Virus Cellular Receptor 2 Human Recombinant, Sf9

Recombinant Human HAVCR2 produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 423 amino acids (aa 22-202) and having a molecular mass of 47.3kDa. (Molecular size on SDS-PAGE will appear at approximately 40-57kDa). HAVCR2 is fused to a 239 amino acid hIgG-His-tag at C-terminus & purified by proprietary chromatographic techniques.

Shipped with Ice Packs
Cat. No.
BT9411
Source
Sf9, Baculovirus cells.
Appearance
Sterile filtered colorless solution.

HAVCR2 Mouse

Hepatitis A Virus Cellular Receptor 2 Mouse Recombinant

HAVCR2 Mouse Recombinant produced in HEK293 cells is a single, glycosylated polypeptide chain (20-193 a.a) containing 413 amino acids and having a molecular mass of 46.3kDa.
HAVCR2 is fused to a 239 amino acid hIgG-His-Tag at C-terminus & purified by proprietary chromatographic techniques.

Shipped with Ice Packs
Cat. No.
BT9471
Source

HEK293 cells.

Appearance

Sterile filtered colorless solution.

Definition and Classification

Hepatitis A is an acute infectious disease of the liver caused by the hepatitis A virus (HAV), a small, non-enveloped RNA virus classified in the genus Hepatovirus within the family Picornaviridae . Unlike hepatitis B and C, hepatitis A does not cause chronic liver disease but can lead to debilitating symptoms and, in rare cases, fulminant hepatitis (acute liver failure), which can be fatal .

Biological Properties

Key Biological Properties: HAV is a small, spherical virus with a diameter of 27-32 nm, containing a single-stranded, positive-sense RNA genome of approximately 7.5 kb . The virus has icosahedral symmetry and lacks an envelope .

Expression Patterns and Tissue Distribution: HAV primarily targets hepatocytes in the liver. The virus attaches to liver cells through an immunoglobulin-like cellular receptor and enters the cell via receptor-mediated endocytosis . Once inside, the viral genome is released into the host’s cytoplasm, leading to hepatocyte damage .

Biological Functions

Primary Biological Functions: HAV causes liver inflammation, affecting the liver’s ability to process nutrients, filter blood, and fight infections . The virus is primarily transmitted through the fecal-oral route, often via contaminated food or water .

Role in Immune Responses and Pathogen Recognition: The immune response to HAV involves the activation of lymphocytes, which engulf the viral antigen and release inflammatory mediators. This stimulates B and T cells to attack the viral antigen, leading to the production of specific antibodies against HAV .

Modes of Action

Mechanisms with Other Molecules and Cells: HAV interacts with hepatocytes by binding to specific receptors on the cell surface, leading to endocytosis and release of the viral genome into the host cell . The virus then hijacks the host’s cellular machinery to replicate and produce viral proteins .

Binding Partners and Downstream Signaling Cascades: The viral RNA is translated into a single polyprotein, which is cleaved into functional viral proteins by the viral protease . These proteins are involved in viral replication and assembly, leading to the production of new virions .

Regulatory Mechanisms

Regulatory Mechanisms Controlling Expression and Activity: The expression of HAV proteins is regulated by the internal ribosomal entry site (IRES) in the 5’ untranslated region (UTR) of the viral RNA . This allows for cap-independent translation of viral proteins .

Transcriptional Regulation and Post-Translational Modifications: The viral polyprotein undergoes post-translational modifications, including cleavage by the viral protease to produce mature viral proteins . These proteins are essential for viral replication and assembly .

Applications

Biomedical Research: HAV is used in research to study viral pathogenesis, immune responses, and the development of antiviral drugs . Animal models, such as nonhuman primates and mice, are instrumental in understanding HAV infection and testing potential therapies .

Diagnostic Tools: Diagnostic tests for HAV include serological assays to detect anti-HAV antibodies and molecular techniques to identify viral RNA . These tools are crucial for diagnosing acute HAV infection and monitoring outbreaks .

Therapeutic Strategies: Vaccination is the most effective strategy for preventing HAV infection . Inactivated HAV vaccines are widely used and provide long-term immunity . Research is ongoing to develop antiviral drugs targeting HAV replication and protein synthesis .

Role in the Life Cycle

Role Throughout the Life Cycle: HAV infection typically occurs in childhood in regions with poor sanitation, leading to asymptomatic or mild illness . In developed countries, infection often occurs in adolescents and adults, causing more severe symptoms . The virus induces lifelong immunity, preventing reinfection .

From Development to Aging and Disease: HAV does not cause chronic infection, but acute infection can lead to significant morbidity, especially in older adults and individuals with underlying health conditions . Vaccination programs have significantly reduced the incidence of HAV infection in many regions .

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