This is a fluorescently labeled version of the probiotic yeast S. boulardii, widely used to treat diarrheal diseases. The addition of GFP allows for the real-time tracking of yeast survival and distribution throughout the digestive tract in animal models.
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 fluorescently labeled version of the probiotic yeast S. boulardii, widely used to treat diarrheal diseases. The addition of GFP allows for the real-time tracking of yeast survival and distribution throughout the digestive tract in animal models. |
| Target | Saccharomyces boulardii |
| Applications | Used to study the "pharmacokinetics" of probiotic yeast. The advantage is the ability to visualize yeast adherence to intestinal walls and its interaction with the host's native bacteria. |
| Product Identity & Gene Details | |
|---|---|
| Chassis Strain | Saccharomyces boulardii |
| Target Gene(s) | GFP |
| Gene Function | GFP (Green Fluorescent Protein) is integrated into the yeast genome, ensuring that the probiotic "glows" under blue light without affecting its natural anti-inflammatory properties. |
| Modification Type | Transgenic expression (Fluorescent labeling) |
| 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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