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Cat# | Products | Swiss Prot# | Size | Price (US$) | Order |
PQ0071 | Recombinant Protein-Clostridium perfringens Alpha toxin (a.a.24 to 398) | Q3HR45 | 100µg | 1195 | |
PQ0072 | Recombinant Protein-Clostridium perfringens Delta toxin (a.a.38 to 318) | B8QGZ7 | 100µg | 1195 | |
PQ0073 | Recombinant Protein-Clostridium perfringens Epsilon toxin (a.a.32 to 328) | Q57398 | 100µg | 1195 | |
PQ0074 | Recombinant Protein-Clostridium perfringens Hyaluronoglucosaminidase Hyaluronidase Mu toxin (a.a.61 to 460) | P26831 | 100µg | 1195 | |
PQ0075 | Recombinant Protein-Clostridium perfringens Iota toxin component Ia (a.a.23 to 454) | Q46220 | 100µg | 1195 | |
PQ0076 | Recombinant Protein-Clostridium perfringens Iota toxin component Ib (a.a.61 to 460) | Q46221 | 100µg | 1195 | |
PQ0077 | Recombinant Protein-Clostridium perfringens Lambda toxin (a.a.25 to 553) | Q46237 | 100µg | 1195 | |
PQ0078 | Recombinant Protein-Clostridium perfringens Necrotic enteritis toxin B NetB (a.a.31 to 322) | A8ULG6 | 100µg | 1195 | |
PQ0079 | Recombinant Protein-Clostridium perfringens Beta2 toxin (a.a.32 to 265) | B1R976 | 100µg | 1195 | |
PQ0080 | Recombinant Protein-Clostridium perfringens Beta-toxin (a.a.28 to 336) | B1BLG4 | 100µg | 1195 | |
RPQ0071 | cDNA-Clostridium perfringens Alpha toxin (a.a.24 to 398) | Q3HR45 | 2µg | 1870 | |
RPQ0072 | cDNA-Clostridium perfringens Delta toxin (a.a.38 to 318) | B8QGZ7 | 2µg | 1400 | |
RPQ0073 | cDNA-Clostridium perfringens Epsilon toxin (a.a.32 to 328) | Q57398 | 2µg | 1480 | |
RPQ0074 | cDNA-Clostridium perfringens Hyaluronoglucosaminidase Hyaluronidase Mu toxin (a.a.61 to 460) | P26831 | 2µg | 1995 | |
RPQ0075 | cDNA-Clostridium perfringens Iota toxin component Ia (a.a.23 to 454) | Q46220 | 2µg | 2155 | |
RPQ0076 | cDNA-Clostridium perfringens Iota toxin component Ib (a.a.61 to 460) | Q46221 | 2µg | 1995 | |
RPQ0077 | cDNA-Clostridium perfringens Lambda toxin (a.a.25 to 553) | Q46237 | 2µg | 2640 | |
RPQ0078 | cDNA-Clostridium perfringens Necrotic enteritis toxin B NetB (a.a.31 to 322) | A8ULG6 | 2µg | 1455 | |
RPQ0079 | cDNA-Clostridium perfringens Beta2 toxin (a.a.32 to 265) | B1R976 | 2µg | 1165 | |
RPQ0080 | cDNA-Clostridium perfringens Beta-toxin (a.a.28 to 336) | B1BLG4 | 2µg | 1540 |
Clostridium perfringens cDNA and recombinant antigen
Clostridium perfringens is a type of bacterium that is commonly found in soil and the intestinal tracts of both humans and animals. While it is usually harmless, in some cases, it can cause severe illness, including food poisoning, gas gangrene, and necrotic enteritis in poultry.
One of the key factors that contribute to the pathogenicity of C. perfringens is the production of various toxins. Alpha toxin, for example, can cause tissue damage and cell death by disrupting the integrity of cell membranes. Delta toxin, Epsilon toxin, and Lambda toxin are also known to cause cell damage and tissue necrosis, leading to a range of symptoms, depending on the affected organ.
Hyaluronidase is an enzyme produced by C. perfringens that can degrade hyaluronic acid, a component of connective tissue in the body. Mu toxin, another enzyme produced by the bacterium, can cause damage to the nerves and muscles, leading to paralysis and other symptoms.
Iota toxin, which is composed of two components, Ia and Ib, can cause cell death and tissue necrosis by disrupting the normal function of cells in the body. Beta2 toxin and Beta toxin are also produced by C. perfringens, which are known to cause tissue damage and contribute to the severity of the infections.
NetB, or Necrotic enteritis toxin B, is a toxin produced by C. perfringens that is responsible for causing necrotic enteritis in poultry. This toxin can cause damage to the gut lining, leading to inflammation, diarrhea, and other symptoms.
The ability of C. perfringens to produce these various toxins is a key factor in the pathogenesis of the bacterium. In many cases, the presence of these toxins can contribute to the severity of the infections, making it more difficult to diagnose and treat.
Researchers are exploring various approaches to target these toxins, including vaccines and therapies that can neutralize the toxins or prevent their production. Understanding the mechanisms and effects of these toxins is essential for the development of effective treatments for C. perfringens infections.
In summary, C. perfringens is a bacterium that can cause severe illness in humans and animals. The production of various toxins, including alpha, delta, epsilon, hyaluronidase, iota, lambda, NetB, and beta toxins, is a key factor in the pathogenesis of the bacterium. Ongoing research is focused on developing effective treatments to target these toxins and improve outcomes for people and animals with C. perfringens infections.
The use of recombinant proteins/cDNA in academic research and therapeutic applications has skyrocketed. However, successful recombinant protein expression in heterologous expression systems depends on various factors, including codon preference, RNA secondary structure, and GC content. 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. Compared to pre-optimization, more experimental results demonstrated that the expression level was dramatically increased, ranging from two to a hundred times depending on the gene.
The cDNA and recombinant antigen can be used in a variety of laboratory tests, including PCR, ELISA, and immunoblotting. These tests can detect the presence of Clostridium perfringens in samples from infected individuals and can also be used to differentiate between different species of Clostridium. Additionally, these tests can also be used to detect the presence of specific toxins produced by Clostridium perfringens, allowing for the diagnosis of specific infections. The use of cDNA and recombinant antigen for the diagnosis of Clostridium perfringens infections is a highly accurate and cost-effective method for diagnosing and managing these infections.
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