BL21(DE3) Competent Cells for Recombinant protein expression | Chemically competent
High-efficiency Chemically competent E. coli cells optimized for Recombinant protein expression, T7 promoter expression, E. coli promoter expression, Protein production with transformation efficiency ≥1 × 10^6 CFU/µg pBR322.
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What are BL21(DE3) Competent Cells?
BL21(DE3) competent cells are optimized E. coli host cells developed for high-efficiency Recombinant protein expression workflows including Recombinant protein expression, T7 promoter expression, E. coli promoter expression, Protein production. These cells support reliable plasmid uptake, stable propagation, and reproducible transformation performance for molecular biology and protein engineering applications.
Why Choose This Strain?
- Transformation efficiency: ≥1 × 10^6 CFU/µg pBR322
- Standard efficiency expression strain
- Supports plasmids up to Standard bacterial expression plasmids
- Stability: lon and ompT protease-deficient background promotes recombinant protein stability
Key Features
- Strain: BL21(DE3)
- Format: 10 × 0.1 mL/tube
- Cell type: Chemically competent
- Insert compatibility: Expression construct-dependent
- Optimized for Recombinant protein expression
Applications
- Recombinant protein expression
- T7 promoter expression
- E. coli promoter expression
- Protein production
Workflow Compatibility
- IPTG-inducible expression
- T7 expression workflows
- Controlled recombinant protein production
- Bacterial expression systems
Specifications
| Genotype | fhuA2 [lon] ompT gal (λ DE3) [dcm] ∆hsdS. [λ DE3 = λ sBamHIo ∆EcoRI-B int::(lacI::PlacUV5::T7 gene1) i21 ∆nin5] |
|---|---|
| Antibiotic Resistance | Depends on transformed plasmid |
| Growth Conditions | SOC recovery; transformed cells can be grown in LB or TB broth and plated on selective LB agar |
| Plasmid Types | T7 expression vectors, E. coli promoter-driven vectors, pET-style vectors, pBR322 |
| Recombination Notes | Not a recA cloning strain; optimized for expression rather than reduced-recombination cloning |
| Max Plasmid Size | Standard bacterial expression plasmids |
Detailed Specifications
| Stability Type | lon and ompT protease-deficient background promotes recombinant protein stability |
|---|---|
| Insert Size Compatibility | Expression construct-dependent |
| Format | 10 × 0.1 mL/tube |
Handling & Protocol
| Transformation Method | Heat shock |
|---|---|
| Protocol Time | ~2 hours to plating, plus overnight incubation |
| Recovery Time | 1 hour at 37°C in SOC |
| Storage Conditions | -80°C |
| Shipping Conditions | Dry ice |
| Shelf Life | ~6 - 12 months at -80°C (typical competent cell stability) |
Industry Comparison
Comparable to BL21(DE3) expression strains for Recombinant protein expression workflows.
Comparable to industry-standard BL21(DE3) expression strains used for IPTG-inducible recombinant protein production from T7 and E. coli promoter-driven vectors.
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Quality Control
- Transformation efficiency validated with control plasmid
- Genotype verified
- Contamination-free
- CoA provided
Key Advantages
- Optimized for recombinant protein expression
- Carries T7 RNA polymerase under IPTG-inducible lacUV5 control
- Compatible with T7 and E. coli promoter-driven constructs
- lon and ompT protease-deficient background supports protein stability
- Suitable for bacterial protein production workflows
Why Researchers Choose Amid Biosciences Competent Cells
- High transformation efficiency for reliable cloning workflows
- Optimized strains for phage display, mutagenesis, and protein engineering
- Stringent quality control testing
- Fast shipping and scientific support
- Research-use-only products manufactured for reproducibility
Related Products
- SS320 Competent Cells for Large Phage Display Libraries
- TG1 Competent Cells for Antibody Phage Display
- DH5α Competent Cells for Routine Cloning
Research Use Only. Not for diagnostic or therapeutic use.