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| Size | 96T |
|---|---|
| Brand | ProteoGenix |
| Product type | Elisa assay kits |
| Product name | HSV-1/HHV-1 gC ELISA Kit |
|---|---|
| Delivery condition | Blue ice (+4°C) |
| Delivery lead time in business days | 3-5 days if in stocks, 3-5 weeks if production is needed |
| Storage condition | 4°C for short term (1 week), store at -20°C to -80°C for long term(1 year); Avoid repeated freeze-thaw cycles |
| Brand | ProteoGenix |
| Note | For research use only. |
| Immunogen | gC |
| Assay type | Quantitative |
| Detection method | Colorimetric |
| Recovery | 80-120% |
The HSV-1/HHV-1 gC ELISA Kit is a highly sensitive and specific diagnostic tool used for the detection of antibodies against the glycoprotein C (gC) of Herpes Simplex Virus type 1 (HSV-1) or Human Herpesvirus type 1 (HHV-1). This kit is widely used in research and clinical settings for the diagnosis and monitoring of HSV-1/HHV-1 infections.
HSV-1/HHV-1 is a double-stranded DNA virus belonging to the Herpesviridae family. The virus is composed of an icosahedral nucleocapsid surrounded by a lipid envelope. The gC protein is a major structural component of the viral envelope and is involved in viral attachment and entry into host cells.
The gC protein is a type I transmembrane glycoprotein with a molecular weight of approximately 120 kDa. It is composed of three distinct domains: an N-terminal domain, a central domain, and a C-terminal domain. The N-terminal domain contains the signal peptide and is responsible for the translocation of the protein to the cell membrane. The central domain is highly conserved among different herpesviruses and is responsible for the binding of gC to heparan sulfate proteoglycans on the surface of host cells. The C-terminal domain is variable in sequence and is responsible for the species-specificity of gC.
The gC protein plays a crucial role in the initial stages of HSV-1/HHV-1 infection. It binds to heparan sulfate proteoglycans on the surface of host cells, facilitating viral attachment and entry. The central domain of gC also interacts with cellular receptors, such as nectin-1, which is essential for the fusion of the viral envelope with the host cell membrane.
In addition to its role in viral entry, gC also has immunomodulatory functions. It can bind to and inhibit the activity of complement proteins, preventing the activation of the host immune response. This allows the virus to evade the immune system and establish a persistent infection.
The HSV-1/HHV-1 gC ELISA Kit is a valuable tool for the diagnosis and monitoring of HSV-1/HHV-1 infections. It is a highly sensitive and specific assay that detects antibodies against gC in patient serum or plasma. The kit is based on the principle of enzyme-linked immunosorbent assay (ELISA), where gC antigen is immobilized on a microplate and patient samples are added. If antibodies against gC are present in the sample, they will bind to the antigen, and the bound antibodies can be detected using a colorimetric reaction.
This kit is widely used in clinical settings for the diagnosis of primary and recurrent HSV-1/HHV-1 infections. It can also be used to differentiate between HSV-1 and HSV-2 infections, as gC is specific to HSV-1. In addition, the kit is used in research settings to study the prevalence and epidemiology of HSV-1/HHV-1 infections in different populations.
The gC protein of HSV-1/HHV-1 has been identified as a potential therapeutic target for the treatment of viral infections. Several studies have shown that targeting gC can inhibit viral entry and replication, making it a promising target for antiviral therapy. Furthermore, gC-specific antibodies have been shown to neutralize viral infectivity, making them potential candidates for the development of a vaccine against HSV-1/HHV-1.
The HSV-1/HHV-1 gC ELISA Kit is also used in research studies to understand the role of gC in viral pathogenesis and host immune response. It is also used to evaluate the efficacy of potential antiviral drugs and vaccines targeting gC. Furthermore, the kit is used in epidemiological studies to determine the prevalence of
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