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NEB Turbo Competent E. coli (High Efficiency) |
 | | | | NEB Turbo Competent E. coli (High Efficiency) | | | |
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Prices are in US dollars and valid only for US orders.
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- Colonies visible after 6.5 hours
- T1 phage resistant (fhuA2)
- Free of animal products
- K12 Strain
Description:
Chemically competent E. coli cells suitable for high efficiency transformation and rapid colony growth.
Reagents Supplied:
C2984H:
20 x 0.05 ml/tube of chemically competent NEB Turbo Competent E.coli cells (Store at -80°C)
20 ml of SOC outgrowth medium (Store at room temperature)
0.025 ml of 50 pg/µl pUC19 Control DNA (Store at -20°C)
C2984I:
6 x 0.2 ml/tube of chemically competent NEB Turbo Competent E. coli cells (Store at ?80°C)
25 ml of SOC outgrowth medium (Store at room temperature)
0.025 ml of 50 pg/µl pUC19 Control DNA (Store at -20°C)
Genotype: F' proA+B+ lacIq ΔlacZM15/fhuA2 Δ(lac-proAB) glnV gal R(zgb-210::Tn10) Tets endA1 thi-1 Δ(hsdS-mcrB)5
Transformation Protocol Variables
Thawing: Cells are best thawed on ice and DNA added as soon as the last bit of ice in the tube disappears. Cells can also be thawed by hand, but warming above 0°C will decrease the transformation efficiency.
Incubation of DNA with Cells on Ice: For maximum transformation efficiency, cells and DNA should be incubated together on ice for 30 minutes. Expect a 2-fold loss in transformation efficiency for every 10 minutes you shorten this step.
Heat Shock: Both the temperature and the timing of the heat shock step are important and specific to the transformation volume and vessel. Using the transformation tube provided, 30 seconds at 42°C is optimal.
Outgrowth: Outgrowth at 37°C for 1 hour is best for cell recovery and for expression of antibiotic resistance. Expect a 2-fold loss in transformation efficiency for every 15 minutes you shorten this step. SOC gives 2-fold higher transformation efficiency than LB medium; and incubation with shaking or rotating the tube gives 2-fold higher transformation efficiency than incubation without shaking.
Plating: Selection plates can be used warm or cold, wet or dry without significantly affecting the transformation efficiency. However, warm, dry plates are easier to spread and allow for the most rapid colony formation.
DNA Effects on Transformation Efficiency and Colony Output: The optimal amount of DNA to use in a transformation reaction is lower than commonly recognized. Using clean, supercoiled pUC19, the efficiency of transformation is highest in the 100 pg-1 ng range. However, the total colonies which can be obtained from a single transformation reaction increase up to about 100 ng.
* Ideally, DNA for transformation should be purified and resuspended in water or TE. However, up to 10 µl of DNA directly from a ligation mix can be used with only a two-fold loss of transformation efficiency. Where it is necessary to maximize the number of transformants (e.g. a library), a purification step, either a spin column or phenol/chloroform extraction and alcohol precipitation should be added.
Advantages:- Transformation efficiency 1-3 x 109 cfu/μg pUC19 DNA
- Tight control of expression by laclq allows potentially toxic genes to be cloned
- Highest growth rate on agar plates - visible colonies 6.5 hours after transformation
- Activity nonspecific endonuclease I (endA) eliminated for highest quality plasmid preparations
- Suitable for blue/white screening by α-complementation of the β-galactosidase gene
- Suitable for 5 minute transformation protocol with AmpR plasmids
- EcoKr-m-, McrBC-
Reaction & Storage Conditions
Storage Temperature:
-80°C
Notes
General notes:- CAUTION: This product contains DMSO, a hazardous material. Review the MSDS before handling.
- STORAGE AND HANDLING: Competent cells should be stored at -80°C. Storage at -20°C will result in a significant decrease in transformation efficiency. Cells lose efficiency whenever they are warmed above -80°C, even if they do not thaw.
FAQs
- How should I calculate the transformation efficiency (C2984)?
- What are the solutions/recipes (C2984)?
- What are the strain properties (C2984)?
Quality Control for Current Lot
Quality control values for a specific lot can be found on the datacard which accompanies each product.
Transformation Efficiency:
100 pg of pUC19 plasmid DNA was used to transform NEB Turbo Competent E.coli following the High Efficiency Protocol provided. Greater than 1-3 x 109 colonies formed/µg after a 12 hour incubation on LB-ampicillin plates at 37°C.
Untransformed cells were also tested for resistance to phage Φ80, a standard test for resistance to phage T1, resistance to nitrofurantoin, and sensitivity to ampicillin, chloramphenicol, kanamycin and tetracycline. They were shown to be suitable for blue/white screening by α-complementation of the β-galactosidase gene using pUC19.
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