S.Enteritidis OmpA Recombinant Protein (RPPB4162)
- SKU:
- RPPB4162
- Product Type:
- Recombinant Protein
- Species:
- Salmonella enteritidis
- Research Area:
- Microbiology
Description
| Product Name: | S.Enteritidis OmpA Recombinant Protein |
| Product Code: | RPPB4162 |
| Size: | 0.5mg |
| Species: | S.Enteritidis |
| Target: | OmpA |
| Synonyms: | Outer Membrane Protein-A, OmpA. |
| Source: | Escherichia Coli |
| Physical Appearance: | Sterile Filtered clear solution. |
| Formulation: | PBS. |
| Stability: | OmpA S.Enteritidis Recombinant although stable at 4°C for 1 week, should be stored below -18°C.�Please prevent freeze thaw cycles. |
| Purity: | Protein is >95% pure as determined by 10% PAGE (coomassie staining). |
The OmpA protein is one of the main outer-membrane proteins of a large array of Gram-negative bacteria such as A.salmonicida, Shigella dysenteriae and E.coli.OmpA�s major physiological functions include maintenance of the structural integrity and morphology of the cells and porin activity, as well as a role in conjugation and bacteriophage binding.Achromogenic atypical Aeromonas salmonicida is the causative agent of goldfish ulcer disease.Virulence of this bacterium is associated with the production of a paracrystalline outer membrane A-layer protein.The species specific structural gene for the monomeric form of A-protein was cloned into a pET-3d plasmid in order to express and produce a recombinant form of the protein in E.coli BL21(DE3). The induced protein was isolated from inclusion bodies by a simple solubilization-renaturation procedure and purified by ion exchange chromatography on Q-Sepharose to over 95% pure monomeric protein.Recombinant A-protein was compared by biochemical, immunological and molecular methods with the A-protein isolated from atypical A.salmonicida bacterial cells by the glycine and the membrane extraction methods.
The Recombinant �Salmonella Enteritidis Outer Membrane Protein A, E.Coli derived, 330 amino acids, contains the ompA immunodominant regions. The protein is fused to a His tag at C-terminal and purified by standard chromatography techniques.
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