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Cat# | Products (Recombinant protein) | Swiss Prot# | Size | Price (US$) | Order |
PL0862 | Recombinant protein-Wolbachia endosymbiont of Aedes polynesiensis Outer surface protein (a.a.21 to 198) | Q4FCP3 | 100 µg | 1195 | |
PL0863 | Recombinant protein-Wolbachia endosymbiont of Dirofilaria immitis Surface protein (a.a.27 to 236) | Q9K4Y6 | 100 µg | 1195 | |
RPL0862 | cDNA-Wolbachia endosymbiont of Aedes polynesiensis Outer surface protein (a.a.21 to 198) | Q4FCP3 | 2 µg | 1062 | |
RPL0863 | cDNA-Wolbachia endosymbiont of Dirofilaria immitis Surface protein (a.a.27 to 236) | Q9K4Y6 | 2 µg | 1254 |
Wolbachia endosymbiont cDNA and recombinant antigen
Wolbachia endosymbiont and outer surface proteins (OSPs) play a crucial role in the survival and transmission of several disease-causing organisms, including Aedes polynesiensis and Dirofilaria immitis. In this article, we will explore the fascinating world of Wolbachia endosymbiont and OSPs in these two important disease vectors and the role they play in the survival and transmission of these organisms.
Wolbachia Endosymbiont in Aedes polynesiensis:
Wolbachia endosymbiont is a fascinating bacterium that infects a wide range of arthropods, including Aedes polynesiensis. In Aedes polynesiensis, Wolbachia endosymbiont plays a crucial role in the reproductive biology of the mosquito. Wolbachia endosymbiont is transmitted vertically from the mother to the offspring and causes cytoplasmic incompatibility, which reduces the fitness of offspring that do not carry the bacterium. This has important implications for the control of mosquito-borne diseases, as the introduction of Wolbachia-infected mosquitoes can reduce the transmission of diseases such as dengue, Zika, and chikungunya.
Outer Surface Proteins in Dirofilaria immitis:
Dirofilaria immitis, commonly known as heartworm, is a parasitic worm that infects dogs and other canids. OSPs are critical components of the outer surface of Dirofilaria immitis and play a crucial role in the survival and transmission of the parasite. The most well-characterized OSP is the Surface Protein, which is involved in the attachment of the parasite to the host’s tissues. The Surface Protein is also a major target of the host’s immune system, and the parasite can evade the immune response by undergoing antigenic variation.
The Pathology of Aedes polynesiensis and Dirofilaria immitis:
Aedes polynesiensis is a significant vector of dengue, Zika, and chikungunya in many Pacific Island countries. The bite of infected Aedes polynesiensis can also cause other diseases, such as filariasis. Dirofilaria immitis causes heartworm disease in dogs, which can lead to severe cardiovascular and respiratory disease and death if left untreated.
Wolbachia endosymbiont and OSPs play a crucial role in the survival and transmission of Aedes polynesiensis and Dirofilaria immitis, two important disease vectors. Understanding the biology of these organisms and the role of these proteins in their survival and transmission is essential for the development of effective control strategies and treatments for these devastating diseases. By exploring the fascinating world of Wolbachia endosymbiont and OSPs, we can better understand the biology of these organisms and the mechanisms by which they cause disease.
The application of Wolbachia endosymbiont cDNA and recombinant antigen expression is a promising research field for understanding the molecular mechanisms of host-microbe interactions. This approach can be used to study how Wolbachia endosymbionts interact with their hosts, their role in the regulation of gene expression, and their potential as vaccine candidates. Furthermore, expression of recombinant antigens can be used to identify and characterize novel antigens and can provide insight into the immune response of the host to Wolbachia endosymbionts. This approach may also be useful for the development of novel vaccines and other therapeutic interventions targeting Wolbachia-associated diseases.
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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