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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PP0832 | Recombinant Protein-Salmonella agona Cpn60 groEL protein (a.a.61 to 545) | B5F2L0 | 100 µg | 1195 | |
PP0833 | Recombinant Protein-Salmonella agona (a.a.20 to 379) | B5EYA5 | 100 µg | 1195 | |
PP0834 | Recombinant Protein-Salmonella agona A (a.a.40 to 371) | B5F1V4 | 100 µg | 1195 | |
PP0835 | Recombinant Protein-Salmonella agona assembly factor yaeT (a.a.61 to 460) | B5F8T8 | 100 µg | 1195 | |
PP0836 | Recombinant Protein-Salmonella agona N (a.a.25 to 372) | B5F607 | 100 µg | 1195 | |
PP0837 | Recombinant Protein-Salmonella agona OMP85 family (a.a.61 to 460) | B5F3D6 | 100 µg | 1195 | |
PP0838 | Recombinant Protein-Salmonella agona Surface antigen domain protein (a.a.30 to 179) | B5F8E2 | 100 µg | 1195 | |
PP0839 | Recombinant Protein-Salmonella agona Surface antigens protein SpaK (a.a.30 to 135) | B5F3X6 | 100 µg | 1195 | |
PP0840 | Recombinant Protein-Salmonella agona Surface antigens protein spaM (a.a.21 to 147) | B5F3X4 | 100 µg | 1195 | |
RPP0832 | cDNA-Salmonella agona Cpn60 groEL protein (a.a.61 to 545) | B5F2L0 | 2 µg | 2420 | |
RPP0833 | cDNA-Salmonella agona (a.a.20 to 379) | B5EYA5 | 2 µg | 1795 | |
RPP0834 | cDNA-Salmonella agona A (a.a.40 to 371) | B5F1V4 | 2 µg | 1655 | |
RPP0835 | cDNA-Salmonella agona assembly factor yaeT (a.a.61 to 460) | B5F8T8 | 2 µg | 1995 | |
RPP0836 | cDNA-Salmonella agona N (a.a.25 to 372) | B5F607 | 2 µg | 1735 | |
RPP0837 | cDNA-Salmonella agona OMP85 family (a.a.61 to 460) | B5F3D6 | 2 µg | 1995 | |
RPP0838 | cDNA-Salmonella agona Surface antigen domain protein (a.a.30 to 179) | B5F8E2 | 2 µg | 800 | |
RPP0839 | cDNA-Salmonella agona Surface antigens protein SpaK (a.a.30 to 135) | B5F3X6 | 2 µg | 800 | |
RPP0840 | cDNA-Salmonella agona Surface antigens protein spaM (a.a.21 to 147) | B5F3X4 | 2 µg | 800 |
Salmonella agonacDNA and recombinant antigen
Salmonella Agona is a bacterium that causes a range of symptoms, from mild gastroenteritis to severe systemic infections. To better understand the mechanisms of infection and develop effective treatments, scientists have been studying various proteins associated with Salmonella Agona, including Cpn60 groEL, assembly factor yaeT, OMP85 family, Surface Antigen Domain Protein, protein SpaK, and SpaM.
Cpn60 groEL Protein: A Chaperonin Involved in Protein Folding
Cpn60 groEL is a chaperonin protein that assists in the folding of other proteins in the cell. In Salmonella Agona, Cpn60 groEL plays a critical role in the assembly and function of flagella, which are essential for motility and virulence. Studies have also shown that Cpn60 groEL is involved in the secretion of effector proteins that aid in the invasion of host cells.
Assembly Factor yaeT: Regulating the Assembly of Outer Membrane Proteins
Outer membrane proteins (OMPs) are crucial for the survival and virulence of Salmonella Agona. Assembly factor yaeT is a protein that regulates the proper assembly of OMPs in the bacterial outer membrane. Studies have shown that disrupting the yaeT gene in Salmonella Agona leads to defects in the assembly of OMPs, which in turn impairs bacterial growth and virulence.
OMP85 Family: Building and Maintaining the Bacterial Outer Membrane
The OMP85 family of proteins is involved in the biogenesis and maintenance of the bacterial outer membrane. In Salmonella Agona, OMP85 proteins play a crucial role in virulence by enabling the bacterium to survive the harsh conditions of the host environment. Studies have also shown that OMP85 proteins are essential for the secretion of virulence factors and the assembly of flagella.
Surface Antigen Domain Protein: A Target for Vaccine Development
Surface Antigen Domain Protein (SapD) is a highly immunogenic protein found on the surface of Salmonella Agona. SapD is essential for bacterial adhesion and invasion of host cells, making it an attractive target for vaccine development. Studies have shown that immunization with SapD can protect mice from lethal Salmonella Agona infection, indicating its potential as a vaccine candidate.
Protein SpaK and SpaM: Regulating the Secretion of Effector Proteins
Proteins SpaK and SpaM are involved in the regulation of the type III secretion system (T3SS) in Salmonella Agona. The T3SS is a virulence mechanism used by the bacterium to inject effector proteins into host cells, which manipulate host cell processes and aid in bacterial survival. Studies have shown that SpaK and SpaM are critical for the efficient secretion of effector proteins and the successful invasion of host cells.
The proteins associated with Salmonella Agona play critical roles in the infection and survival of the bacterium. By understanding the functions and interactions of these proteins, researchers can develop new strategies for treating and preventing Salmonella Agona infections. From chaperonins involved in protein folding to surface proteins that are targets for vaccines, each protein presents a unique opportunity for combating this dangerous pathogen.
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 cDNA and recombinant antigen of S. agona can be used in various applications for diagnosis, research, and vaccine development.
Diagnostic Tests: cDNA of S. agona can be used in molecular diagnostic tests to detect the presence of the bacterium in a patient’s sample or in food samples. This can be done by amplifying a specific genetic target using polymerase chain reaction (PCR) and detecting the amplified product using fluorescence or other methods.
Research: cDNA of S. agona can be used in research studies to investigate the genetic characteristics and pathogenesis of the bacterium. Recombinant antigens can also be used to study the immune response to S. agona infections, to identify potential vaccine candidates, and to develop new diagnostic tests.
Vaccine Development: Recombinant antigens of S. agona can be used to develop vaccines against the bacterium. These vaccines can stimulate the production of specific antibodies that recognize and neutralize S. agona.
In conclusion, the cDNA and recombinant antigen of S. agona have important applications in the field of diagnostics, research, and vaccine development, and can help in the development of new and more effective ways to prevent and treat foodborne illness caused by this bacterium.
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