Products

Shigella sonnei cDNA and Antigen

Cat#

Product Name

Swiss Prot#

Size

Price (US$)

Order

PP0880

Recombinant Protein-Shigella sonnei Invasion plasmid antigen (a.a.17 to 107)

Q1PD17

100 µg

1195

Order

PP0881

Recombinant Protein-Shigella sonnei Surface antigens spaM Spa13 protein (a.a.21 to 112)

P0A1K4

100 µg

1195

Order

PP0882

Recombinant Protein-Shigella sonnei Surface antigens protein spaN Spa 32 (a.a.22 to 292)

P0A1K6

100 µg

1195

Order

PP0883

Recombinant Protein-Shigella sonnei Surface antigens protein spaO Spa 33 protein (a.a.52 to 293)

P0A1L0

100 µg

1195

Order

PP0884

Recombinant Protein-Shigella sonnei Surface antigens protein spaP Spa 24 protein (a.a.21 to 216)

P0A1L4

100 µg

1195

Order

PP0885

Recombinant Protein-Shigella sonnei Surface antigens protein spaR Spa 29 protein (a.a.21 to 256)

P0A1M7

100 µg

1195

Order

PP0886

Recombinant Protein-Shigella sonnei Surface antigens protein spaS Spa 40 protein (a.a.21 to 342)

P0A1M9

100 µg

1195

Order

PP0887

Recombinant Protein-Shigella sonnei IpaA (a.a.49 to 449)

Q3YTQ5

100 µg

1195

Order

PP0888

Recombinant Protein-Shigella sonnei IpgB2 (a.a.21 to 188)

Q3YTW8

100 µg

1195

Order

RPP0880

cDNA-Shigella sonnei Invasion plasmid antigen (a.a.17 to 107)

Q1PD17

2 µg

800

Order

RPP0881

cDNA-Shigella sonnei Surface antigens spaM Spa13 protein (a.a.21 to 112)

P0A1K4

2 µg

800

Order

RPP0882

cDNA-Shigella sonnei Surface antigens protein spaN Spa 32 (a.a.22 to 292)

P0A1K6

2 µg

1350

Order

RPP0883

cDNA-Shigella sonnei Surface antigens protein spaO Spa 33 protein (a.a.52 to 293)

P0A1L0

2 µg

1205

Order

RPP0884

cDNA-Shigella sonnei Surface antigens protein spaP Spa 24 protein (a.a.21 to 216)

P0A1L4

2 µg

975

Order

RPP0885

cDNA-Shigella sonnei Surface antigens protein spaR Spa 29 protein (a.a.21 to 256)

P0A1M7

2 µg

1175

Order

RPP0886

cDNA-Shigella sonnei Surface antigens protein spaS Spa 40 protein (a.a.21 to 342)

P0A1M9

2 µg

1605

Order

RPP0887

cDNA-Shigella sonnei IpaA (a.a.49 to 449)

Q3YTQ5

2 µg

2000

Order

RPP0888

cDNA-Shigella sonnei IpgB2 (a.a.21 to 188)

Q3YTW8

2 µg

835

Order

Shigella sonnei 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

Shigella sonnei is a bacterium that causes shigellosis, a gastrointestinal disease that affects millions of people worldwide. Shigella sonnei uses a variety of virulence factors to invade and colonize the human intestinal tract. One of the most important virulence factors is the invasion plasmid antigen (ipa) system, which includes several surface antigens, including SpaM, Spa13, SpaN, Spa32, Spa33, Spa24, Spa29, Spa40, IpaA, and IpgB2.

The SpaM protein is an important surface antigen of Shigella sonnei that is involved in bacterial invasion of host cells. Spa13 is another surface antigen that has been shown to play a role in bacterial motility and invasion. The SpaN and Spa32 proteins are involved in the secretion of Ipa proteins, which are important for bacterial invasion of host cells.

The Spa33 protein is an important component of the Shigella sonnei needle complex, which is responsible for the secretion of Ipa proteins into host cells. The Spa24 protein is also involved in the secretion of Ipa proteins and has been shown to be required for bacterial invasion of host cells. The Spa29 and Spa40 proteins are additional components of the needle complex that are important for the secretion of Ipa proteins.

IpaA is an important virulence factor of Shigella sonnei that is involved in bacterial invasion of host cells. IpgB2 is another virulence factor that has been shown to play a role in bacterial invasion and colonization of the intestinal tract.

Overall, the invasion plasmid antigen (ipa) system, including the various surface antigens and virulence factors, is critical for the pathogenesis of Shigella sonnei and its ability to cause shigellosis. Understanding the function of these virulence factors may lead to the development of novel therapeutics or vaccines for the prevention and treatment of this important gastrointestinal 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 use of cDNA and recombinant antigens derived from Shigella sonnei can have various applications in the fields of molecular biology, biotechnology, and medicine. Some of these applications include:

Diagnostic tests: Recombinant antigens can be used in the development of rapid diagnostic tests for the detection of Shigella sonnei in clinical samples. These tests can help to quickly identify the presence of the bacteria and provide early treatment for infected individuals.

Vaccine development: Recombinant antigens can be used in the development of vaccines against Shigella sonnei. By exposing the immune system to specific antigens, the body can build immunity to the bacteria, reducing the risk of infection.

Study of bacterial pathogenesis: The use of cDNA from Shigella sonnei can help researchers to study the genetic basis of the bacteria’s pathogenesis. By analyzing the cDNA, researchers can identify the genes and gene products involved in the bacteria’s ability to cause disease, which can lead to the development of new treatments and preventions.

Bacterial evolution and evolution of antibiotic resistance: The use of cDNA from Shigella sonnei can help researchers to study the evolution of the bacteria and the evolution of antibiotic resistance. By analyzing the cDNA, researchers can identify genetic changes that occur in the bacteria over time, which can provide insights into the evolution of antibiotic resistance and the development of new treatments.

Overall, the use of cDNA and recombinant antigens from Shigella sonnei has the potential to contribute to a better understanding of the bacteria and its role in disease, as well as to the development of new diagnostic tools and treatments for bacterial infections.

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