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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PP0404 | Recombinant Protein-Giardia muris Variant-specific surface protein 01 (a.a.32 to 235) | Q49L31 | 100 µg | 1195 | |
PP0405 | Recombinant Protein-Giardia muris Variant-specific surface protein 02 (a.a.17 to 255) | Q49L30 | 100 µg | 1195 | |
PP0406 | Recombinant Protein-Giardia muris Variant-specific surface protein 03 (a.a.11 to 235) | Q49L29 | 100 µg | 1195 | |
PP0407 | Recombinant Protein-Giardia muris Variant-specific surface protein 04 (a.a.21 to 347) | Q49L28 | 100 µg | 1195 | |
PP0408 | Recombinant Protein-Giardia muris Variant-specific surface protein 05 (a.a.33 to 235) | Q49L27 | 100 µg | 1195 | |
PP0409 | Recombinant Protein-Giardia muris Variant-specific surface protein 06 (a.a.17 to 373) | Q49L26 | 100 µg | 1195 | |
RPP0404 | cDNA-Giardia muris Variant-specific surface protein 01 (a.a.32 to 235) | Q49L31 | 2 µg | 1015 | |
RPP0405 | cDNA-Giardia muris Variant-specific surface protein 02 (a.a.17 to 255) | Q49L30 | 2 µg | 1190 | |
RPP0406 | cDNA-Giardia muris Variant-specific surface protein 03 (a.a.11 to 235) | Q49L29 | 2 µg | 1120 | |
RPP0407 | cDNA-Giardia muris Variant-specific surface protein 04 (a.a.21 to 347) | Q49L28 | 2 µg | 1630 | |
RPP0408 | cDNA-Giardia muris Variant-specific surface protein 05 (a.a.33 to 235) | Q49L27 | 2 µg | 1010 | |
RPP0409 | cDNA-Giardia muris Variant-specific surface protein 06 (a.a.17 to 373) | Q49L26 | 2 µg | 1780 |
Giardia muris cDNA and recombinant antigen
Giardia muris is a species of parasitic protozoa that is found in the gastrointestinal tract of mice, rats, and other rodents. This species is closely related to Giardia lamblia, which is a common cause of diarrhea in humans. G. muris is not known to be a human pathogen, but it may be an animal model for studying the mechanisms of giardiasis and the development of treatments. G. muris replicates within the host’s gut and is transmitted through the ingestion of contaminated food or water. Symptoms associated with G. muris infection include diarrhea, vomiting, weight loss, and abdominal pain. Treatment typically consists of antibiotics, antiparasitic drugs, and supportive care.
Variant-specific surface proteins (VSPs) are a family of surface-exposed proteins that are crucial for the pathogenicity of certain parasites, including the protozoan parasites Giardia lamblia and Trypanosoma brucei. These parasites use VSPs to evade the host immune response and establish chronic infections.
In Giardia lamblia, VSPs are expressed on the surface of trophozoites, which are the active, replicating form of the parasite. The parasite can switch the expression of VSPs between different variants, allowing it to evade the host immune response and establish a chronic infection. VSPs are also involved in the formation of cysts, which are the dormant, infective form of the parasite.
In Trypanosoma brucei, VSPs are expressed on the surface of bloodstream forms of the parasite, which are the form of the parasite that circulates in the bloodstream of the host. The parasite can switch the expression of VSPs between different variants, allowing it to evade the host immune response and establish a chronic infection. VSPs are also involved in antigenic variation, which is the process by which the parasite changes the expression of surface antigens to evade the host immune response.
The significance of VSPs as surface proteins that evade immune responses lies in their potential as diagnostic and therapeutic targets. Because VSPs are highly immunogenic and specific to the parasite, they can be used as biomarkers for the detection of infection. Several studies have investigated the use of VSPs as diagnostic markers for Giardia lamblia and Trypanosoma brucei infections, with promising results.
In addition to their potential as diagnostic targets, VSPs may also have potential as therapeutic targets. Because VSPs are involved in the pathogenesis of these parasites, targeting VSPs may be an effective strategy for the development of new therapies against these infections. Several studies have investigated the use of VSPs as vaccine candidates for Giardia lamblia and Trypanosoma brucei infections, with promising results.
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.
Some of these applications are:
Identification and characterization of virulence factors: The cDNA of G. muris can be used to study the expression of genes involved in virulence and pathogenesis. This information can aid in the development of new treatments for giardiasis.
Diagnostic tests: Recombinant antigens of G. muris can be used as target antigens in diagnostic tests such as ELISA (Enzyme-linked Immunosorbent Assay) for the detection of giardiasis in animals and humans.
Vaccine development: The recombinant antigens of G. muris can be used as potential vaccine targets to protect against giardiasis.
Antibiotic resistance studies: The cDNA of G. muris can be used to study the expression of genes involved in drug resistance, which can help in the development of new drugs to combat drug-resistant strains of this parasite.
These are just a few examples of the applications of G. muris cDNA and recombinant antigen. Further research in this field can lead to the development of new and effective treatments for giardiasis and improve our understanding of the biology of this parasite.
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