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Competent Cells for DNA Library Construction
Competent cells with very high transformation efficiencies are used for DNA library construction (such as cDNA, gDNA, phage display, and CRISPR and gene libraries) to promote high coverage of unique constructs. Electroporation is a preferred transformation method to create DNA fragment and gene libraries because it provides the highest transformation efficiency. Competent cells for heat-shock transformation are also available.
How critical is transformation efficiency for getting good DNA library representation
E. coli strains for plasmid library construction
These competent cells have mutated mcrA, mcrBC, mrr, and/or hsdRMS restriction systems so they are efficient at cloning methylated DNA, which is important for construction of highly representative eukaryotic genomic libraries.
The following Invitrogen competent cells feature:
- Blue/white colony selection
- High transformation efficiency
Electrocompetent bacteria for library preparation
| Product |  |  |  |  |
|---|---|---|---|---|
| ElectroMAX DH10B Competent Cells | ElectroMAX Stbl4 Competent Cells | ElectroMAX DH10B T1 Phage-Resistant Competent Cells | MegaX DH10B T1R Electrocompetent Cells | |
| Recommended for | gDNA and plasmid rescue | Inverted and direct repeats, CRISPR libraries | gDNA and plasmid rescue (phage resistance) | Large DNA inserts, highest efficiency |
| Transformation Efficiency | >1 x 1010 cfu/µg | >5 x 109 cfu/µg | >1 x 1010 cfu/µg | >3 x 1010 cfu/µg (highest) |
| Compatible plasmid size | >20 kb | >100 kb | >20 kb | >100 kb |
| T1, T5, and φ80 phage resistance (tonA (fhuA)) | – | – | ||
| Generating ssDNA (Contains F´ episome) | – | – | – | |
| Cloning unstable inserts | – | – | – | |
| M13mp18 RF DNA included | – | – | – | – |
| Format | 5 x 100 µL/tube | 5 x 100 µL/tube | 5 x 100 µL/tube | 5 x 100 µL/tube |
Chemically competent bacteria for library preparation
| Product |  |  |
|---|---|---|
| MAX Efficiency DH5αF´IQ Competent Cells | OmniMAX 2 T1R chemically competent E. coli | |
| Recommended for | Phage display, toxic gene cloning | Gateway and TOPO cloning reactions |
| Transformation Efficiency | >1 x 108 cfu/µg | >5 x 109 cfu/µg |
| Compatible plasmid size | >20 kb | >20 kb |
| T1, T5, and φ80 phage resistance (tonA (fhuA)) | – | |
| Generating ssDNA (Contains F´ episome) | ||
| Cloning unstable inserts | – | – |
| M13mp18 RF DNA included | – | |
| Format | 5 x 200 µL/tube | 21 x 50 uL/tube |
Electrocompetent bacteria for library preparation
| Product | | | | |
|---|---|---|---|---|
| ElectroMAX DH10B Competent Cells | ElectroMAX Stbl4 Competent Cells | ElectroMAX DH10B T1 Phage-Resistant Competent Cells | MegaX DH10B T1R Electrocompetent Cells | |
| Recommended for | gDNA and plasmid rescue | Inverted and direct repeats, CRISPR libraries | gDNA and plasmid rescue (phage resistance) | Large DNA inserts, highest efficiency |
| Transformation Efficiency | >1 x 1010 cfu/µg | >5 x 109 cfu/µg | >1 x 1010 cfu/µg | >3 x 1010 cfu/µg (highest) |
| Compatible plasmid size | >20 kb | >100 kb | >20 kb | >100 kb |
| T1, T5, and φ80 phage resistance (tonA (fhuA)) | – | – | ||
| Generating ssDNA (Contains F´ episome) | – | – | – | |
| Cloning unstable inserts | – | – | – | |
| M13mp18 RF DNA included | – | – | – | – |
| Format | 5 x 100 µL/tube | 5 x 100 µL/tube | 5 x 100 µL/tube | 5 x 100 µL/tube |
Chemically competent bacteria for library preparation
| Product | | |
|---|---|---|
| MAX Efficiency DH5αF´IQ Competent Cells | OmniMAX 2 T1R chemically competent E. coli | |
| Recommended for | Phage display, toxic gene cloning | Gateway and TOPO cloning reactions |
| Transformation Efficiency | >1 x 108 cfu/µg | >5 x 109 cfu/µg |
| Compatible plasmid size | >20 kb | >20 kb |
| T1, T5, and φ80 phage resistance (tonA (fhuA)) | – | |
| Generating ssDNA (Contains F´ episome) | ||
| Cloning unstable inserts | – | – |
| M13mp18 RF DNA included | – | |
| Format | 5 x 200 µL/tube | 21 x 50 uL/tube |
Phage display library construction
Phage display libraries are used to discover antibodies [1] and have been used to identify human antibodies against SARS-CoV-2 [2]. In addition to high transformation efficiency competent cells, phage display protocols require a M13KO7 Helper Phage that can be acquired separately.
CRISPR library construction
CRISPR screening workflows often require construction of sgRNA libraries. Stbl4 competent cells have been used to successfully build these RNA libraries [3].
Preparing cDNA and genomic DNA libraries
Thermo Fisher Scientific provides many reagents and resources for bacterial library construction. cDNA can be constructed using the Invitrogen Second Strand cDNA Synthesis Kit or other cDNA library construction kits.
For genomic DNA library preparation, use Invitrogen genomic DNA extraction kits to consistently achieve excellent results.
Tips for transforming bacteria for construction of DNA libraries
Still not sure which competent cells are right for construction of your DNA library?
References
- Ledsgaard L., Kilstrup M., Karatt-Vellatt A., et al. (2018) Basics of Antibody Phage Display Technology. Toxins (Basel) 236. doi:10.3390/toxins10060236
- Wu Y., Li C., Xia S., et al. (2020) Identification of Human Single-Domain Antibodies against SARS-CoV-2. Cell Host & Microbe 891. doi:10.1016/j.chom.2020.04.023
- Read A., Gao S., Batchelor E., et al. (2017) Flexible CRISPR library construction using parallel oligonucleotide retrieval. Nucleic Acids Res 45. doi:10.1093/nar/gkx181
Competent cells: Featured products
In addition to competent cells, we offer a broad suite of products for the cloning workflow.
Microbial
media
Explore types of bacterial growth media to use for cloning, plasmid DNA preparation, and protein expression.
Electroporation
cuvettes
Learn more about universal-fit electroporation cuvettes for use with competent cells.
TOPO PCR
cloning kits
Learn more about one-step PCR cloning that combines traditional restriction and ligation cloning.
Gibson Assembly
cloning kits
Gibson Assembly cloning kits provide highly efficient, seamless cloning, enabling the assembly of multiple DNA fragments of varying lengths into any vector.
Resources
Have any questions on competent cells or transformation? Click on the resources listed below to access overviews, videos, genotype guides, and educational resources.
Review rich educational content on transformation workflow, troubleshooting, strategies, and selection guides.
Stay up-to-date on industry trends in molecular cloning with on-demand webinars.
Short articles and digital handbook for cloning applications
Access white papers and technical and application notes on molecular cloning.
Watch instructional videos on troubleshooting tips, how-to videos, and explainers related to molecular cloning.
Get support for your cloning experiments
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