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Cat# | Products (Recombinant protein) | Swiss Prot# | Size | Price (US$) | Order |
PL0859 | Recombinant protein-Trypanosoma vivax Surface glycoprotein (a.a.55 to 391) | Q27114 | 100 µg | 1195 | |
PL0860 | Recombinant protein-Trypanosoma vivax Diagnostic antigen (a.a.21 to 107) | Q27103 | 100 µg | 1195 | |
PL0861 | Recombinant protein-Trypanosoma vivax Diagnostic antigen (a.a.21 to 111) | Q27111 | 100 µg | 1195 | |
RPL0859 | cDNA-Trypanosoma vivax Surface glycoprotein (a.a.55 to 391) | Q27114 | 2 µg | 2016 | |
RPL0860 | cDNA-Trypanosoma vivax Diagnostic antigen (a.a.21 to 107) | Q27103 | 2 µg | 800 | |
RPL0861 | cDNA-Trypanosoma vivax Diagnostic antigen (a.a.21 to 111) | Q27111 | 2 µg | 800 |
Trypanosoma vivax cDNA and recombinant antigen
Trypanosoma vivax is a parasitic protozoan that causes animal trypanosomiasis, a disease that affects domestic and wild animals, particularly cattle, sheep, and goats. The disease is prevalent in many countries in Africa, South America, and Asia, and has a significant impact on animal health, welfare, and productivity. In this article, we will explore the Surface Glycoprotein (SGP) in Trypanosoma vivax and its importance as a key diagnostic antigen for the detection and control of the disease.
The Importance of Surface Glycoprotein:
The SGP is a critical component of the surface coat of Trypanosoma vivax and plays a crucial role in the immune evasion and survival of the parasite within the host. The SGP undergoes antigenic variation, meaning that the expression of different SGP genes leads to the generation of antigenically distinct parasite populations. This allows the parasite to evade the host’s immune system continuously. The SGP is also essential for the survival of the parasite within the host by protecting it from the host’s immune system.
The SGP is a key diagnostic antigen for the detection and control of Trypanosoma vivax infection. The SGP can be used in serological tests to detect antibodies against the parasite in the blood of infected animals. Serological tests are essential for the early detection of the disease and for the identification of infected animals, which can help prevent the spread of the disease to other animals. The SGP can also be used in vaccine development, as it is a highly conserved antigen that is essential for parasite survival.
The Pathology of Trypanosoma vivax:
Trypanosoma vivax causes a range of pathological effects in the host, including anemia, weight loss, and reduced productivity. The parasite can also cross the blood-brain barrier and cause neurological symptoms, such as depression, incoordination, and paralysis. Trypanosoma vivax is primarily transmitted by the bite of infected tsetse flies, which are found in many parts of Africa.
Trypanosoma vivax is a significant threat to animal health and welfare in many parts of the world, particularly in developing countries. The SGP is a critical component of the surface coat of the parasite and plays a crucial role in the immune evasion and survival of the parasite within the host. The SGP is also a key diagnostic antigen for the detection and control of Trypanosoma vivax infection. Understanding the biology of Trypanosoma vivax and the role of the SGP in the pathology of the parasite is essential for the development of effective control strategies and treatments for this devastating disease.
This cDNA and recombinant antigen can be used to detect antibodies to T. vivax in cattle. The cDNA and recombinant antigen can be used to measure the number of antibodies present in the sera of cattle, which can then be used to determine if the animal is infected with T. vivax. The cDNA and recombinant antigen can also be used to detect the presence of T. vivax in the tissues of cattle, which can help to differentiate between the active and inactive stages of the parasite. This cDNA and recombinant antigen can also be used in combination with other diagnostic tests, such as PCR and ELISA, to improve the accuracy of the diagnosis of trypanosomiasis in cattle.
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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