Products

Bartonella Quintana cDNA and Antigen

Cat#

Product Name

Swiss Prot#

Size

Price (US$)

Order

PP0080

Recombinant Protein-Bartonella quintana15kDa antigen (a.a.29 to 104)

Q4L2Q6

100 µg

1195

Order

PP0081

Recombinant Protein-Bartonella quintana 17kDa antigen (a.a.27 to 148)

Q9K2U8

100 µg

1195

Order

PP0082

Recombinant Protein-Bartonella quintana Antigen Lipoptrotein(a.a.30 to 391)

Q6G034

100 µg

1195

Order

PP0083

Recombinant Protein-Bartonella quintana(a.a.29 to 104)

Q8KQC3

100 µg

1195

Order

PP0084

Recombinant Protein-Bartonella quintana60 kDa chaperonin Cpn60 (a.a.61 to 547)

O33964

100 µg

1195

Order

RPP0080

cDNA-Bartonella quintana 15kDa antigen (a.a.29 to 104)

Q4L2Q6

2 µg

800

Order

RPP0081

cDNA-Bartonella quintana 17kDa antigen (a.a.27 to 148)

Q9K2U8

2 µg

800

Order

RPP0082

cDNA-Bartonella quintana Antigen Lipoptrotein(a.a.30 to 391)

Q6G034

2 µg

1805

Order

RPP0083

cDNA-Bartonella quintana Type IV secretion system protein virB2 (a.a.29 to 104)

Q8KQC3

2 µg

800

Order

RPP0084

cDNA-Bartonella quintana 60 kDa chaperonin Cpn60 (a.a.61 to 547)

O33964

2 µg

2430

Order

Bartonella quintana 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

Bartonella quintana is a gram-negative bacterium that is the causative agent of trench fever, a disease that was first described during World War I among soldiers in trenches. Trench fever is characterized by fever, headache, muscle pain, and a rash, and is typically transmitted to humans through the bite of infected lice. In addition to trench fever, B. quintana has also been associated with endocarditis, bacteremia, and other diseases. The bacterium has a complex life cycle that allows it to persist and persistently infect hosts, making it a challenging pathogen to control. Further research on the biology and virulence of B. quintana can help improve diagnosis and treatment of trench fever and other diseases associated with this bacterium.

An antigen is a molecule that is recognized by the immune system and triggers an immune response. Antigens are typically proteins or polysaccharides and are found on the surface of pathogens, including bacteria like Bartonella quintana. In the case of B. quintana, antigens play a crucial role in the host-pathogen interaction and are involved in the bacterium’s ability to evade the host immune response. Identification of B. quintana antigens can lead to the development of effective diagnostic tests and vaccines to prevent trench fever and other diseases associated with this bacterium.

Bartonella quintana produces several important antigens that play a role in the pathogenesis of this bacterium. These include the 15kDa antigen, 17kDa antigen, Lipoprotein antigen, and the 60 kDa chaperonin Cpn60.

The 15kDa antigen is a highly immunogenic protein that has been identified as a major antigenic component of B. quintana. It has been shown to stimulate the production of antibodies that can be detected in the serum of infected individuals, making it a valuable diagnostic marker.

The 17kDa antigen is a protein that is highly conserved among Bartonella species and is known to be involved in the adherence of B. quintana to endothelial cells. This antigen has been shown to elicit a strong immune response and is also used as a diagnostic marker.

The Lipoprotein antigen is a surface protein that is known to be involved in the attachment of B. quintana to host cells. It has been shown to be highly immunogenic and is thought to be an important target for the development of vaccines and other therapeutic strategies.

The 60 kDa chaperonin Cpn60 is a highly conserved protein that is involved in the folding and assembly of other proteins. It has been shown to be highly immunogenic and may play a role in the pathogenesis of B. quintana by eliciting an immune response.

In conclusion, the various antigens of Bartonella quintana, including the 15kDa antigen, 17kDa antigen, Lipoprotein antigen, and the 60 kDa chaperonin Cpn60, play important roles in the pathogenesis of this bacterium. Understanding the role of these antigens is essential for developing effective diagnostic, therapeutic, and preventive strategies for diseases caused by this organism.

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 Bartonella quintana 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 Bartonella quintana, including the identification of genes involved in resistance and the evaluation of the expression of these genes.

Vaccine development: The recombinant antigens of Bartonella quintana 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 Bartonella quintana in clinical specimens, such as blood, lymph node aspirates, and wound swabs.

Serological assays: The recombinant antigens of Bartonella quintana 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 Bartonella quintana infections.

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