Products

Mobiluncus curtisii cDNA and recombinant antigen

Cat#

Product Name

Swiss Prot#

Size

Price (US$)

Order

PP0493

Recombinant Protein-Mobiluncus curtisii Pathogen-specific surface antigen (a.a.25 to 216)

C2BVR6

100 µg

1195

Order

PP0494

Recombinant Protein-Mobiluncus curtisii 60 kDa chaperonin (a.a.61 to 542)

C2BT56

100 µg

1195

Order

PP0495

Recombinant Protein-Mobiluncus curtisii cell surface protein (a.a.61 to 460)

C2BUV4

100 µg

1195

Order

RPP0493

cDNA-Mobiluncus curtisii Pathogen-specific surface antigen (a.a.25 to 216)

C2BVR6

2 µg

955

Order

RPP0494

cDNA-Mobiluncus curtisii 60 kDa chaperonin (a.a.61 to 542)

C2BT56

2 µg

2405

Order

RPP0495

cDNA-Mobiluncus curtisii cell surface protein (a.a.61 to 460)

C2BUV4

2 µg

1995

Order

Mobiluncus curtisii 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

Mobiluncus curtisii is a Gram-negative anaerobic bacterium that can be found in the vaginal microbiota of women. It has been associated with bacterial vaginosis; a common vaginal infection characterized by an imbalance in the vaginal microbiota. Recent studies have identified key pathogen-specific surface antigens of Mobiluncus curtisii, including a 60 kDa chaperonin and a cell surface protein, which have the potential to be used in developing targeted diagnostic and treatment strategies for Mobiluncus curtisii infections.

60 kDa chaperonin: The 60 kDa chaperonin is a protein antigen produced by Mobiluncus curtisii. Chaperonins are a type of molecular chaperone that play a crucial role in protein folding and stability. The 60 kDa chaperonin of Mobiluncus curtisii has been identified as a key pathogen-specific surface antigen, and it has been proposed as a potential target for developing diagnostic tests specific to Mobiluncus curtisii. Antibodies generated against this antigen may be used in diagnostic assays to detect the presence of Mobiluncus curtisii in clinical samples, helping to improve the accuracy of diagnosis.

Cell surface protein: The cell surface protein of Mobiluncus curtisii is another key pathogen-specific surface antigen that has been identified in recent studies. This protein is located on the outer surface of the bacterium and is involved in various cellular functions, including adhesion to host tissues and evasion of host immune responses. The cell surface protein of Mobiluncus curtisii has the potential to be used as a target for developing diagnostic tests and treatment strategies specific to this bacterium. Antibodies or other targeted therapeutic agents that can specifically recognize and bind to this protein may be used to develop targeted treatment approaches for Mobiluncus curtisii infections.

The use of these key pathogen-specific surface antigens of Mobiluncus curtisii in diagnostic tests and targeted treatment strategies has the potential to improve the accuracy and specificity of diagnosis, as well as the effectiveness of treatment for Mobiluncus curtisii infections. Further research and validation studies are needed to fully understand the clinical utility of these antigens and optimize their diagnostic and therapeutic applications. It’s important to consult with healthcare professionals for accurate diagnosis and management of Mobiluncus curtisii infections.

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 application of Mobiluncus curtisii cDNA and recombinant antigen in vaccine development could potentially be used to prevent or reduce the incidence of BV. By using cDNA and recombinant antigens, vaccine developers can create a vaccine that would stimulate the body’s immune system to produce antibodies against Mobiluncus curtisii. These antibodies would then bind to the bacteria and prevent it from attaching to the vaginal wall and causing an infection. Furthermore, because the cDNA and recombinant antigens are derived from the bacterial genome, they would provide a more specific target for the vaccine, thus increasing its effectiveness. This type of vaccine could be especially useful in developing countries where BV is more common as it could provide a relatively inexpensive and effective way to reduce the incidence of BV.

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