Products

Theileria Yamaguchi cDNA and recombinant antigen

Cat#

Products (Recombinant protein)

Swiss Prot#

Size

Price (US$)

Order

PL0773

Recombinant protein-Theileria Yamaguchi Sika Deer Piroplasm major immunodominant protein (a.a.21 to 136)

A8CYL0

100 µg

1195

Order

RPL0773

cDNA-Theileria Yamaguchi Sika Deer Piroplasm major immunodominant protein (a.a.21 to 136)

A8CYL0

2 µg

690

Order

Theileria Yamaguchi 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

Theileria Yamaguchi is a protozoan parasite that infects sika deer and causes theileriosis, a tick-borne disease. This disease is common in Japan, China, and Korea, and has been recently reported in the United States.

Piroplasm major is an important molecule involved in Theileria Yamaguchi pathogenesis.

Piroplasm Major: A Key Component of Theileria Yamaguchi Infection
Piroplasm major is a highly conserved protein that is expressed on the surface of Theileria Yamaguchi piroplasms. It is involved in host cell invasion and immune evasion and is a potential vaccine candidate due to its immunogenicity and involvement in pathogenesis.

Recent studies have shown that Piroplasm major plays a critical role in Theileria Yamaguchi pathogenesis by facilitating host cell invasion and modulating the host immune response. It also interacts with other parasite molecules to facilitate parasite survival and proliferation within the host.

Understanding the Molecular Basis of Theileria Yamaguchi Pathogenesis
Theileria Yamaguchi pathogenesis is a complex process that involves multiple molecules and pathways. The parasite uses a variety of mechanisms to evade the host immune response, establish a persistent infection, and cause disease.

Piroplasm major is a critical component of Theileria Yamaguchi pathogenesis and targeting this molecule could pave the way for the development of effective vaccines and control strategies.

Theileria Yamaguchi cDNA and recombinant antigens can be used for a variety of applications. These include diagnosis and treatment of Theileria-induced diseases, as well as vaccine development and research into the biology and pathogenesis of the parasite.

Diagnosis: Theileria Yamaguchi cDNA and recombinant antigens can be used for detection of the parasite in clinical samples. This is done by detecting specific gene sequences in a sample, which can be used to identify the presence of the parasite.

Treatment: Theileria Yamaguchi cDNA and recombinant antigens can also be used in the treatment of Theileria-induced diseases. Specific gene sequences can be used to identify the presence of the parasite, and then specific drugs can be used to target the parasite and eliminate it from the body.

Vaccine development: Theileria Yamaguchi cDNA and recombinant antigens can also be used for vaccine development. Specific gene sequences can be used to identify the presence of the parasite and then used to develop vaccines that will protect against the parasite.

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.

 

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