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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PP0901 | Recombinant Protein-Staphylococcus haemolyticus Antigen 67 kDa (a.a.61 to 591) | C2LZC1 | 100 µg | 1195 | |
PP0902 | Recombinant Protein-Staphylococcus haemolyticus Immunodominant antigen B (a.a.36 to 170) | C2LZI8 | 100 µg | 1195 | |
PP0903 | Recombinant Protein-Staphylococcus haemolyticus Immunodominant staphylococcal antigen B (a.a.36 to 173) | C2LZ89 | 100 µg | 1195 | |
PP0904 | Recombinant Protein-Staphylococcus haemolyticus Secretory antigen SsaA (a.a.25 to 272) | Q4L487 | 100 µg | 1195 | |
PP0905 | Recombinant Protein-Staphylococcus haemolyticus Similar to immunodominant antigen B (a.a.36 to 161) | Q4L351 | 100 µg | 1195 | |
PP0906 | Recombinant Protein-Staphylococcus haemolyticus Similar to secretory antigen SsaA (a.a.31 to 144) | Q4L954 | 100 µg | 1195 | |
PP0907 | Recombinant Protein-Staphylococcus haemolyticus Staphylococcal secretory antigen ssaA2 (a.a.28 to 258) | C2LWZ6 | 100 µg | 1195 | |
RPP0901 | cDNA-Staphylococcus haemolyticus Antigen 67 kDa (a.a.61 to 591) | C2LZC1 | 2 µg | 2650 | |
RPP0902 | cDNA-Staphylococcus haemolyticus Immunodominant antigen B (a.a.36 to 170) | C2LZI8 | 2 µg | 800 | |
RPP0903 | cDNA-Staphylococcus haemolyticus Immunodominant staphylococcal antigen B (a.a.36 to 173) | C2LZ89 | 2 µg | 800 | |
RPP0904 | cDNA-Staphylococcus haemolyticus Secretory antigen SsaA (a.a.25 to 272) | Q4L487 | 2 µg | 1235 | |
RPP0905 | cDNA-Staphylococcus haemolyticus Similar to immunodominant antigen B (a.a.36 to 161) | Q4L351 | 2 µg | 800 | |
RPP0906 | cDNA-Staphylococcus haemolyticus Similar to secretory antigen SsaA (a.a.31 to 144) | Q4L954 | 2 µg | 800 | |
RPP0907 | cDNA-Staphylococcus haemolyticus Staphylococcal secretory antigen ssaA2 (a.a.28 to 258) | C2LWZ6 | 2 µg | 1150 |
Staphylococcus haemolyticus cDNA and recombinant antigen
Staphylococcus haemolyticus is a bacterium that is commonly found on human skin and mucous membranes. It is considered a commensal organism, but it can also cause infections, particularly in immunocompromised patients or those with medical devices. To cause infections, S. haemolyticus has developed a variety of virulence factors, including antigen 67 kDa, immunodominant antigen B, staphylococcal antigen B, secretory antigen SsaA, and similar proteins to these antigens.
Antigen 67 kDa is a protein of S. haemolyticus that is involved in the binding of host cells and the formation of biofilms. It is considered an important virulence factor, as it allows S. haemolyticus to adhere to host tissues and evade the immune system.
Immunodominant antigen B and staphylococcal antigen B are surface proteins of S. haemolyticus that are known to elicit an immune response in humans. They are considered potential vaccine candidates due to their ability to induce protective antibodies in animal models. Research has also shown that these antigens are expressed in most S. haemolyticus strains, suggesting that they may play conserved roles in the biology of this bacterium.
Secretory antigen SsaA and similar proteins are involved in the secretion of proteins into the extracellular environment. They are considered important virulence factors, as they are involved in the formation of biofilms and the colonization of host tissues. Research has also shown that these antigens are involved in the regulation of genes that are important for the survival of S. haemolyticus under stress conditions.
Staphylococcal secretory antigen SsaA2 is another protein of S. haemolyticus that is involved in the secretion of proteins into the extracellular environment. It is considered an important virulence factor, as it is involved in the formation of biofilms and the colonization of host tissues.
Overall, antigen 67 kDa, immunodominant antigen B, staphylococcal antigen B, secretory antigen SsaA, and similar proteins to these antigens, as well as staphylococcal secretory antigen SsaA2, are important virulence factors of S. haemolyticus. Understanding the function of these proteins may lead to the development of novel therapeutics or vaccines for the prevention and treatment of S. haemolyticus infections.
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.
The use of cDNA (complementary DNA) and recombinant antigens derived from Staphylococcus haemolyticus can have various applications in the fields of molecular biology, biotechnology, and medicine. Some of these applications include:
Diagnostic tests: Recombinant antigens can be used in the development of rapid diagnostic tests for the detection of Staphylococcus haemolyticus in clinical samples. These tests can help to quickly identify the presence of the bacteria and provide early treatment for infected individuals.
Vaccine development: Recombinant antigens can be used in the development of vaccines against Staphylococcus haemolyticus. By exposing the immune system to specific antigens, the body can build immunity to the bacteria, reducing the risk of infection.
Study of bacterial pathogenesis: The use of cDNA from Staphylococcus haemolyticus can help researchers to study the genetic basis of the bacteria’s pathogenesis. By analyzing the cDNA, researchers can identify the genes and gene products involved in the bacteria’s ability to cause disease, which can lead to the development of new treatments and preventions.
Bacterial evolution and evolution of antibiotic resistance: The use of cDNA from Staphylococcus haemolyticus can help researchers to study the evolution of the bacteria and the evolution of antibiotic resistance. By analyzing the cDNA, researchers can identify genetic changes that occur in the bacteria over time, which can provide insights into the evolution of antibiotic resistance and the development of new treatments.
Overall, the use of cDNA and recombinant antigens from Staphylococcus haemolyticus has the potential to contribute to a better understanding of the bacteria and its role in disease, as well as to the development of new diagnostic tools and treatments for bacterial infections.
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