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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PN0028 | Recombinant Protein-Avian encephalomyelitis virus Structural protein VP1 (a.a.21 to 270) | Q6S4P2 | 100 µg | 1195 | |
PN0029 | Recombinant Protein-Avian encephalomyelitis virus Protein VP2 (a.a.20 to 242) | Q6R325 | 100 µg | 1195 | |
PN0030 | Recombinant Protein-Avian encephalomyelitis virus Protein VP3 (a.a.243 to 487) | Q6R325 | 100 µg | 1195 | |
PN0031 | Recombinant Protein-Avian encephalomyelitis virus Protein VP1 (a.a.488 to 757) | Q6R325 | 100 µg | 1195 | |
PN0032 | Recombinant Protein-Avian encephalomyelitis virus Protein 2B (a.a.807 to 1021) | Q6R325 | 100 µg | 1195 | |
PN0033 | Recombinant Protein-Avian encephalomyelitis virus Picornain 3C (a.a.1434 to 1648) | Q6R325 | 100 µg | 1195 | |
RPN0028 | cDNA-Avian encephalomyelitis virus Structural protein VP1 (a.a.21 to 270) | Q6S4P2 | 2 µg | 1245 | |
RPN0029 | cDNA-Avian encephalomyelitis virus Protein VP2 (a.a.20 to 242) | Q6R325 | 2 µg | 1110 | |
RPN0030 | cDNA-Avian encephalomyelitis virus Protein VP3 (a.a.243 to 487) | Q6R325 | 2 µg | 1220 | |
RPN0031 | cDNA-Avian encephalomyelitis virus Protein VP1 (a.a.488 to 757) | Q6R325 | 2 µg | 1345 | |
RPN0032 | cDNA-Avian encephalomyelitis virus Protein 2B (a.a.807 to 1021) | Q6R325 | 2 µg | 1070 | |
RPN0033 | cDNA-Avian encephalomyelitis virus Picornain 3C (a.a.1434 to 1648) | Q6R325 | 2 µg | 1070 |
Avian encephalomyelitis virus cDNA and recombinant antigen
Avian Encephalomyelitis virus (AEV) is a pathogen that infects poultry, causing a disease known as avian encephalomyelitis. It is a member of the Alphavirus genus in the Togaviridae family and primarily affects the central nervous system of birds, leading to symptoms such as paralysis, tremors, and death. Transmission of AEV occurs through the oral route and it is commonly spread through contaminated feed, water, or equipment. The disease can have a significant impact on the poultry industry, causing economic losses and trade restrictions. Control measures include vaccination, biosecurity, and proper sanitation.
AEV genome is a single-stranded RNA molecule that contains genetic information encoding for the virus’s structural and non-structural proteins. It is approximately 11.7 kilobases in length and is classified as a positive-sense RNA virus. The AEV genome codes for six non-structural proteins and three structural proteins, including the viral envelope glycoproteins that are involved in the immune response and viral replication. The genome is replicated in the cytoplasm of infected cells and serves as a template for the synthesis of new virus particles. Understanding the genetic structure and replication of AEV is important for the development of effective vaccines and antiviral strategies.
The Avian Encephalomyelitis virus antigen refers to any substance present on the surface of the virus that elicits an immune response in a host. Antigens can be proteins, carbohydrates, or other molecules. In the case of AEV, the viral envelope glycoproteins are the primary antigens that trigger an immune response. Antibodies generated against these antigens can neutralize the virus and protect the host from infection. Vaccines against AEV often use inactivated or weakened forms of the virus or its antigens to stimulate the immune system and provide immunity against future infection.
Structural protein VP1 is the major component of the virus capsid, and is involved in virus attachment, entry, and protection of the viral genome. Protein VP2 is involved in virus assembly and release, while VP3 is involved in virus stability.
Protein 2B is a transmembrane protein that plays a role in viral replication and host cell membrane modification. It is also involved in the inhibition of host immune responses, which allows the virus to evade detection and clearance by the host.
Picornain 3C is a viral protease that is involved in the processing of the viral polyprotein, which is essential for the replication of the virus. It is also involved in the inhibition of host immune responses, which allows the virus to establish infection in the host.
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.
Avian encephalomyelitis virus (AEV) cDNA and recombinant antigens have potential applications in the fields of biotechnology and vaccine development. In biotechnology, recombinant AEV proteins and cDNAs can be used to create novel biopharmaceuticals and gene therapy products. They can also be used to produce transgenic animals, as well as to develop diagnostic tests and vaccines. In vaccine development, recombinant AEV antigens can be used to elicit an immune response in individuals, which can then be used to prevent or reduce the severity of AEV infections. Additionally, AEV cDNA can be used to create recombinant viruses, which can be used in vaccine development and as research tools.
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