This is a specialized therapeutic strain engineered to express and secrete the Sj16 protein, a peptide derived from a parasite (Schistosoma japonicum). This strain is designed to act as a "living immunomodulator" to treat inflammatory diseases.
For Research Use Only. Not intended for use in food manufacturing or medical procedures (diagnostics or therapeutics). Do Not Use in Humans.
| Product Information | |
|---|---|
| Product Overview | This is a specialized therapeutic strain engineered to express and secrete the Sj16 protein, a peptide derived from a parasite (Schistosoma japonicum). This strain is designed to act as a "living immunomodulator" to treat inflammatory diseases. |
| Target | Escherichia coli Nissle 1917 |
| Applications | Used for the treatment of Inflammatory Bowel Disease (IBD) or autoimmune conditions. The advantage is that the probiotic delivers the anti-inflammatory peptide directly to the inflamed gut tissue, reducing systemic side effects. |
| Product Identity & Gene Details | |
|---|---|
| Chassis Strain | Escherichia coli Nissle 1917 |
| Target Gene(s) | Sj16 |
| Gene Function | A 16-kDa protein secreted by helminth parasites that has potent anti-inflammatory and immunosuppressive properties, particularly in the gut. |
| Modification Type | Heterologous protein expression (Anti-inflammatory therapy) |
| Genetic Architecture | |
|---|---|
| Promoter System | Constitutive or Inducible |
| Selection Marker | Standard Antibiotic Marker or Markerless/Scarless (No resistance genes) |
| Delivery & Service Standards | |
|---|---|
| Deliverables | Glycerol Stocks |
| Shipping Conditions | Dry Ice Shipping |
| Lead Time | 4-8 weeks |
| Documents | Certificate of Analysis (COA) or Project Report |
| Verification | PCR Sequencing |
| Engineered Strain Recovery & Handling | |
|---|---|
| Immediate Post-Delivery Steps | 1. Transfer to Storage: Immediately transfer the cryovials to a -80°C ultra-low temperature freezer. 2. Avoid Fluctuations: Do not store the vials in a "frost-free" freezer, as the temperature cycles can damage the cell membranes of the engineered strains. |
| Strain Recovery Protocol | To ensure maximum viability, follow this standard recovery procedure: 1. Preparation: Prepare the appropriate selective agar medium (e.g., LB agar + specific antibiotic as listed in the COA). 2. Partial Thawing (The "Scratch" Method): * Place the cryovial on dry ice. Do not thaw the entire vial. Use a sterile inoculation loop or pipette tip to "scratch" a small amount of ice from the surface of the frozen stock. 3. Streaking: Streak the cells onto the selective agar plate to obtain single colonies. 4. Incubation: Invert the plate and incubate at the specified temperature (e.g., 37°C for E. coli or 30°C for S. cerevisiae) for 16-24 hours. 5. Subculturing: Pick a single, well-isolated colony to inoculate into liquid media for your experiments. |
| Usage Precautions & Best Practices | |
|---|---|
| Antibiotic Pressure | 1. Maintenance: For strains containing plasmids or specific resistance markers, always use the correct concentration of antibiotics in both solid and liquid media to prevent plasmid loss or contamination. 2. Markerless Strains: If the strain is a "scarless" integrated knockout, antibiotic pressure is not required for maintenance, but periodic genotypic verification is recommended. |
| Induction Conditions | 1. If your strain uses an inducible promoter (e.g., T7/IPTG or Arabinose), ensure the culture reaches the optimal OD600 (typically 0.6-0.8) before adding the inducer. 2. Verify the optimal induction temperature, as engineered strains often produce better results at lower temperatures (e.g., 16-25°C) to prevent inclusion body formation. |
| Disposal | All waste (vials, tips, plates) must be autoclaved at 121°C for at least 20 minutes or chemically disinfected before disposal. |
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For Research Use Only. Not intended for use in food manufacturing or medical procedures (diagnostics or therapeutics). Do Not Use in Humans.
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