Products

Rickettsia japonica cDNA and Antigen

Cat#

Product Name

Swiss Prot#

Size

Price (US$)

Order

PP0807

Recombinant Protein-Rickettsia japonica 17 kDa protein (a.a.25 to 107)

Q06DN2

100 µg

1195

Order

PP0808

Recombinant Protein-Rickettsia japonica Citrate synthase (a.a.39 to 411)

Q59742

100 µg

1195

Order

PP0809

Recombinant Protein-Rickettsia japonica B rOmp B Cell surface antigen 5 (a.a.36 to 436)

O06653

100 µg

1195

Order

PP0810

Recombinant Protein-Rickettsia japonica Surface antigen (a.a.31 to 430)

Q3L8Q1

100 µg

1195

Order

RPP0807

cDNA-Rickettsia japonica 17 kDa protein (a.a.25 to 107)

Q06DN2

2 µg

800

Order

RPP0808

cDNA-Rickettsia japonica Citrate synthase (a.a.39 to 411)

Q59742

2 µg

1860

Order

RPP0809

cDNA-Rickettsia japonica B rOmp B Cell surface antigen 5 (a.a.36 to 436)

O06653

2 µg

2000

Order

RPP0810

cDNA-Rickettsia japonica Surface antigen (a.a.31 to 430)

Q3L8Q1

2 µg

1995

Order

Rickettsia japonica cDNA and recombinant antigen

  • Codon-optimized cDNA is cloned into E. coli expression vector with 6x His-tag at N-terminus and ready-to-use for recombinant protein production.
  • Recombinant protein applications: Western Blot may be used for other applications determined by the user.
  • Protein Purity: >90%, as determined by SDS-PAGE under reducing conditions.
  • Protein Activity: N/A
  • Protein Tag:  Contains A 6x histidine tag at N-terminus.
  • Protein Formulation: Liquid
  • Source: Produced from E. coli

Rickettsia japonica is a species of Gram-negative bacteria that is responsible for causing Japanese spotted fever in humans. This disease is primarily transmitted through tick bites and can lead to severe symptoms if left untreated. Understanding the role of cell surface antigens in the pathogenesis of Rickettsia japonica infection is crucial for identifying and preventing the spread of the disease.

One of the most important cell surface antigens in Rickettsia japonica is the 17 kDa protein. This antigen is highly immunogenic and is recognized by antibodies in the sera of infected individuals. The 17 kDa protein is involved in adhesion to host cells and invasion, and it is considered a potential target for developing diagnostic tests and vaccines.

Citrate synthase is another cell surface antigen of Rickettsia japonica that has been studied. This enzyme is involved in the citric acid cycle and plays a crucial role in the metabolism of the bacterium. It is also highly immunogenic and has been used as a marker for the detection of Rickettsia infection.

B rOmp B is a cell surface antigen that is specific to Rickettsia species. This antigen is involved in adhesion to host cells and plays a crucial role in the pathogenesis of Rickettsia infection. It is also highly immunogenic and has been used as a target for developing diagnostic tests and vaccines.

Other cell surface antigens of Rickettsia japonica that have been studied include Sca1, Sca2, Sca3, Sca7, Sca8, Sca9, Sca10, Sca11, Sca12, and Sca13. These antigens are involved in adhesion to host cells, invasion, and the pathogenesis of Rickettsia infection. They are also highly immunogenic and have potential applications in the development of diagnostic tests and vaccines.

In conclusion, understanding the role of cell surface antigens in the pathogenesis of Rickettsia japonica infection is crucial for identifying and preventing the spread of the disease. The 17 kDa protein, citrate synthase, B rOmp B, and other surface antigens of Rickettsia japonica have potential applications in the development of diagnostic tests and vaccines, which could aid in the early detection and prevention of this disease.

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 antigen of R. japonica can be used in various applications for diagnosis, research, and vaccine development.

Diagnostic Tests: cDNA of R. japonica can be used in molecular diagnostic tests to detect the presence of the bacterium in a patient’s sample. 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 R. japonica 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 R. japonica infections, to identify potential vaccine candidates, and to develop new diagnostic tests.

Vaccine Development: Recombinant antigens of R. japonica can be used to develop vaccines against the bacterium. These vaccines can stimulate the production of specific antibodies that recognize and neutralize R. japonica.

In conclusion, the cDNA and recombinant antigen of R. japonica 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 spotted fever rickettsiosis caused by this bacterium.

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