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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PN0323 | Recombinant Protein-Eastern equine encephalitis virus E2 glycoprotein (a.a.50 to 420) | A9XR35 | 100 µg | 1195 | |
PN0324 | Recombinant Protein-Eastern equine encephalitis virus Capsid (a.a.21 to 124) | B4YJI9 | 100 µg | 1195 | |
PN0325 | Recombinant Protein-Eastern equine encephalitis virus E1 glycoprotein (a.a.21 to 209) | B4YK03 | 100 µg | 1195 | |
PN0326 | Recombinant Protein-Eastern equine encephalitis virus capsid (a.a.1 to 261) | A1YZ44 | 100 µg | 1195 | |
PN0327 | Recombinant Protein-Eastern equine encephalitis virus E2 (a.a.325 to 744) | A1YZ44 | 100 µg | 1195 | |
PN0328 | Recombinant Protein-Eastern equine encephalitis virus E1 (a.a.802 to 1242) | A1YZ44 | 100 µg | 1195 | |
PN0329 | Recombinant Protein-Eastern equine encephalitis virus Structural protein E2 (a.a.50 to 420) | Q2PQD4 | 100 µg | 1195 | |
PN0330 | Recombinant Protein-Eastern equine encephalitis virus capsid (a.a.31 to 261) | Q88790 | 100 µg | 1195 | |
PN0331 | Recombinant Protein-Eastern equine encephalitis virus E2 (a.a.325 to 744) | Q9PZX7 | 100 µg | 1195 | |
PN0332 | Recombinant Protein-Eastern equine encephalitis virus E1 (a.a.802 to 1242) | Q9PZX7 | 100 µg | 1195 | |
RPN0323 | cDNA-Eastern equine encephalitis virus E2 glycoprotein (a.a.50 to 420) | A9XR35 | 2 µg | 1850 | |
RPN0324 | cDNA-Eastern equine encephalitis virus Capsid (a.a.21 to 124) | B4YJI9 | 2 µg | 800 | |
RPN0325 | cDNA-Eastern equine encephalitis virus E1 glycoprotein (a.a.21 to 209) | B4YK03 | 2 µg | 940 | |
RPN0326 | cDNA-Eastern equine encephalitis virus capsid (a.a.1 to 261) | A1YZ44 | 2 µg | 1300 | |
RPN0327 | cDNA-Eastern equine encephalitis virus E2 (a.a.325 to 744) | A1YZ44 | 2 µg | 2095 | |
RPN0328 | cDNA-Eastern equine encephalitis virus E1 (a.a.802 to 1242) | A1YZ44 | 2 µg | 2200 | |
RPN0329 | cDNA-Eastern equine encephalitis virus Structural protein E2 (a.a.50 to 420) | Q2PQD4 | 2 µg | 1850 | |
RPN0330 | cDNA-Eastern equine encephalitis virus capsid (a.a.31 to 261) | Q88790 | 2 µg | 1150 | |
RPN0331 | cDNA-Eastern equine encephalitis virus E2 (a.a.325 to 744) | Q9PZX7 | 2 µg | 2095 | |
RPN0332 | cDNA-Eastern equine encephalitis virus E1 (a.a.802 to 1242) | Q9PZX7 | 2 µg | 2200 |
Eastern equine encephalitis virus cDNA and recombinant antigen
Eastern equine encephalitis virus (EEEV) is a virus in the family Togaviridae that can cause severe and often fatal encephalitis (inflammation of the brain) in humans, horses, and other animals. EEEV is primarily transmitted to humans by infected mosquitoes, and symptoms of infection can range from mild flu-like symptoms to severe encephalitis. EEEV infection can cause significant morbidity and mortality, especially in young children and the elderly. The virus is widely distributed in the Eastern and Gulf Coastal regions of the United States and parts of South America, and outbreaks of EEEV disease occur sporadically. There is no specific treatment for EEEV infection, but supportive care, such as maintaining fluid balance, can help manage symptoms. Prevention measures include avoiding exposure to mosquitoes, using insect repellent, and wearing protective clothing. The development of a vaccine for EEEV is an important area of research, but progress has been limited due to the lack of a suitable animal model for the disease. Improving our understanding of the EEEV virus, including its biology, epidemiology, and potential for transmission, is critical for the development of effective diagnostic tools, treatments, and vaccines for this virus.
The Eastern equine encephalitis virus (EEEV) genome refers to the complete genetic material of the virus. The EEEV genome is a positive-sense, single-stranded RNA molecule and is one of the largest RNA virus genomes known. The genetic information encoded in the EEEV genome is critical for the virus’s replication and pathogenesis, and provides important information for understanding the virus’s biology, evolution, and potential for transmission. The EEEV genome has been the subject of extensive study, with the goal of understanding the molecular mechanisms underlying its replication and pathogenesis. This information can be useful for the development of diagnostic tools, treatments, and vaccines for EEEV infection. Studying the EEEV genome can also help to better understand the evolution and diversity of the virus, which can have important implications for the epidemiology and control of the disease.
Eastern equine encephalitis virus (EEEV) antigen refers to specific molecules or substances in the virus that trigger an immune response. Antigens are recognized by the immune system and can be used to diagnose an infection by detecting antibodies produced in response to the virus. In the case of EEEV, antigens may include viral proteins or other components of the virus. Detection of EEEV antigens can be used to diagnose an active infection, especially in people who have not yet developed a significant immune response. Antigen tests for EEEV are generally faster and less expensive than other forms of testing, such as PCR, but may not be as sensitive. The development of a vaccine for EEEV often focuses on targeting specific antigens of the virus that are critical for replication or pathogenesis. Understanding the specific antigens of EEEV is an important area of research for the development of diagnostic tests, treatments, and vaccines for this virus.
The genome of EEEV encodes several viral proteins, including:
E2 glycoprotein: This is a viral envelope glycoprotein that is involved in viral attachment and entry into host cells. It interacts with host cell surface receptors to facilitate viral entry.
Capsid: This is the protein shell that encloses the viral RNA genome, forming the nucleocapsid.
E1 glycoprotein: This is another viral envelope glycoprotein that is involved in viral entry into host cells. It mediates the fusion of the viral envelope with the host cell membrane, allowing the viral nucleocapsid to enter the host cell.
Understanding the structures and functions of these proteins is crucial for the development of effective treatments and preventive measures against EEEV. There are currently no specific antiviral treatments available for EEEV, and the development of effective vaccines is challenging due to the high genetic variability of the virus. However, continued research into the structures and functions of these proteins may lead to the development of new treatments and vaccines against EEEV.
In addition to vaccines and antiviral treatments, effective mosquito control measures are also critical for the prevention and control of EEEV. Mosquitoes are the primary vectors for the virus, and the reduction of mosquito populations and the use of personal protective measures can help to reduce the risk of infection.
The use of recombinant proteins/cDNA in academic research and therapeutic applications has skyrocketed. However, in heterologous expression systems, successful recombinant protein expression is dependent on a variety of factors, including codon preference, RNA secondary structure, and GC content. When compared to pre-optimization, more and more experimental results demonstrated that the expression level was dramatically increased, ranging from two to hundred times depending on the gene. Bioclone has created a proprietary technology platform that has resulted in the creation of over 6,000 artificially synthesized codon-optimized cDNA clones (cloned in E. coli expression Vector), which are ready for production of the recombinant proteins.
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