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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PP0135 | Recombinant Protein-Borrelia garinii Antigen S2-related protein (a.a.28 to 224) | Q662K6 | 100 µg | 1195 | |
PP0136 | Recombinant Protein-Borrelia garinii Antigen P35 (a.a.33 to 348) | B8F1N6 | 100 µg | 1195 | |
PP0137 | Recombinant Protein-Borrelia garinii Antigen P35 (a.a.37 to 285) | Q6ASF2 | 100 µg | 1195 | |
PP0138 | Recombinant Protein-Borrelia garinii Antigen S1(a.a.21 to 397) | B8F2H1 | 100 µg | 1195 | |
PP0139 | Recombinant Protein-Borrelia garinii Antigen S2 (a.a.23 to 281) | B8F1I0 | 100 µg | 1195 | |
PP0140 | Recombinant Protein-Borrelia garinii Basic membrane protein A Immunodominant antigen P39 (a.a.34 to 337) | B7XT52 | 100 µg | 1195 | |
PP0141 | Recombinant Protein-Borrelia garinii p35 surface antigen (a.a.32 to 467) | Q5W291 | 100 µg | 1195 | |
PP0142 | Recombinant Protein-Borrelia garinii surface antigen (a.a.30 to 139) | B8F1P6 | 100 µg | 1195 | |
PP0143 | Recombinant Protein-Borrelia garinii PBi Surface antigen (a.a.61 to 460) | Q9K5F7 | 100 µg | 1195 | |
PP0144 | Recombinant Protein-Borrelia garinii PBr Outer surface 22 kDa lipoprotein Antigen ipla7 (a.a.23 to 195) | B7XT34 | 100 µg | 1195 | |
RPP0135 | cDNA-Borrelia garinii Antigen S2-related protein (a.a.28 to 224) | Q662K6 | 2 µg | 980 | |
RPP0136 | cDNA-Borrelia garinii Antigen P35 (a.a.33 to 348) | B8F1N6 | 2 µg | 1575 | |
RPP0137 | cDNA-Borrelia garinii Antigen P35 (a.a.37 to 285) | Q6ASF2 | 2 µg | 1240 | |
RPP0138 | cDNA-Borrelia garinii Antigen S1 (a.a.21 to 397) | B8F2H1 | 2 µg | 1880 | |
RPP0139 | cDNA-Borrelia garinii Antigen S2 (a.a.23 to 281) | B8F1I0 | 2 µg | 1290 | |
RPP0140 | cDNA-Borrelia garinii Basic membrane protein A Immunodominant antigen P39 (a.a.34 to 337) | B7XT52 | 2 µg | 1515 | |
RPP0141 | cDNA-Borrelia garinii p35 surface antigen (a.a.32 to 467) | Q5W291 | 2 µg | 2175 | |
RPP0142 | cDNA-Borrelia garinii surface antigen (a.a.30 to 139) | B8F1P6 | 2 µg | 800 | |
RPP0143 | cDNA-Borrelia garinii PBi Surface antigen (a.a.61 to 460) | Q9K5F7 | 2 µg | 1995 | |
RPP0144 | cDNA-Borrelia garinii PBr Outer surface 22 kDa lipoprotein Antigen ipla7 (a.a.23 to 195) | B7XT34 | 2 µg | 860 |
Borrelia garinii cDNA and recombinant antigen
Borrelia garinii is a species of spirochete bacteria belonging to the Borrelia genus. It is commonly found in Eurasia and is the primary cause of Lyme disease in Europe and Asia. Symptoms of Lyme Disease caused by B. garinii include fever, headache, joint pain, and a rash. In severe cases, it can cause meningitis, encephalitis, and arthritis. Treatment for Lyme disease caused by B. garinii usually involves antibiotics such as doxycycline, amoxicillin, and cefuroxime. Vaccines are also available for some countries.
Borrelia Garinii affects both humans and animals. One of the most important aspects of understanding this bacterium is to understand the various antigens that it produces. In this article, we will explore some of the key Borrelia Garinii antigens and their roles.
Antigen S2-Related Protein
Antigen S2-Related Protein is a type of protein produced by Borrelia Garinii that plays a crucial role in its survival. It is an essential component of the bacterial cell wall and helps the bacterium to evade the immune system by inhibiting the host’s immune response.
Antigen P35
Antigen P35 is another important protein produced by Borrelia Garinii. It is involved in the formation of the outer membrane of the bacterium and is critical for its survival. Antigen P35 is also an immunodominant antigen, which means that it triggers a strong immune response from the host’s immune system.
Antigen S1 and Antigen S2
Antigen S1 and Antigen S2 are two related proteins that are produced by Borrelia Garinii. They are both involved in the formation of the bacterial cell wall and are essential for its survival. Like Antigen P35, they are also immunodominant antigens.
Basic Membrane Protein A
Basic Membrane Protein A is another crucial component of the Borrelia Garinii cell wall. It helps to maintain the structural integrity of the cell wall and is involved in the transport of nutrients into the bacterium. It is also an immunodominant antigen, meaning that it triggers a strong immune response from the host’s immune system.
Immunodominant Antigen P39
Immunodominant Antigen P39 is a protein produced by Borrelia Garinii that is critical for its survival. It is involved in the formation of the bacterial cell wall and helps the bacterium to evade the host’s immune system. Like the other antigens discussed in this article, it is also an immunodominant antigen.
Garinii P35 Surface Antigen, Garinii Surface Antigen, and PBi Surface Antigen
Garinii P35 Surface Antigen, Garinii Surface Antigen, and PBi Surface Antigen are all different types of surface antigens produced by Borrelia Garinii. They are involved in the formation of the outer membrane of the bacterium and are critical for its survival. These antigens are also immunodominant, meaning that they trigger a strong immune response from the host’s immune system.
PBr Outer Surface 22 kDa Lipoprotein Antigen and Antigen Ipla7
PBr Outer Surface 22 kDa Lipoprotein Antigen and Antigen Ipla7 are two other important antigens produced by Borrelia Garinii. They are both involved in the formation of the outer membrane of the bacterium and are essential for its survival. These antigens are also immunodominant, meaning that they trigger a strong immune response from the host’s immune system.
Understanding the various antigens produced by Borrelia Garinii is crucial for understanding the bacterium’s survival and its ability to cause Lyme disease. By understanding the roles of the various antigens, researchers may be able to develop more effective treatments and vaccines for Lyme disease. It is also important to note that while these antigens are critical for the survival of Borrelia Garinii, they are also the targets of the host’s immune system, making them potential targets for diagnostic tests and therapies
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 (complementary DNA) and recombinant antigens of Borrelia garinii have various applications in the fields of molecular biology and infectious disease, including:
Gene expression analysis: The cDNA can be used as a template to synthesize complementary RNA (cRNA) which can then be used for microarray or RNA sequencing (RNA-seq) analysis to study gene expression patterns in the bacterium under different conditions.
Antimicrobial resistance studies: The cDNA can be used to study the mechanisms of antibiotic resistance in Borrelia garinii, including the identification of genes involved in resistance and the evaluation of the expression of these genes.
Vaccine development: The recombinant antigens of Borrelia garinii can be used to develop subunit vaccines against the bacterium. These antigens can stimulate the immune system to mount a response against the pathogen.
Diagnostics: The cDNA can be used to develop real-time PCR (polymerase chain reaction) assays for the rapid and sensitive detection of Borrelia garinii in clinical specimens, such as blood, synovial fluid, and cerebrospinal fluid.
Serological assays: The recombinant antigens of Borrelia garinii can be used to develop serological assays, such as ELISA (enzyme-linked immunosorbent assay), to detect the presence of antibodies against the bacterium in human or animal serum. These assays can be used for the diagnosis of Borrelia garinii infections.
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