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NEB® 5-alpha Competent E. coli (Subcloning Efficiency)

Catalog # Concentration Size List Price Quantity Your Price
C2988J 6 x 0.4 ml $115.00
$103.50
Catalog # Size List Price Your Price
C2988J 6 x 0.4 ml $115.00
$103.50
Catalog #
Qty:
 
*On-line ordering is for Canadian customers only. Web pricing is applicable only to orders placed online at www.neb.ca

NEB 5-alpha Competent E. coli is a derivative of the popular DH5α. It is T1 phage resistant and endA deficient for high-quality plasmid preparations. 

  • Ideal for subcloning efficiency transformations, such as plasmid transformation or routine subcloning
  • No dry ice surcharge on competent cell shipments
  • Free of animal products
  • High efficiency chemical and electrocompetent formats are also available
Featured Videos
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  • Monarch_MiniprepProtocol_VideoThumb
    Fast transformation plating with glass beads
Chemically competent E. coli cells suitable for subcloning efficiency transformations, such as plasmid transformation or routine subcloning (e.g,. inserting a 1 kb fragment into a 2 kb vector). The efficiency of these cells is not sufficiently high for most other cloning applications. For that, we recommend NEB® 5-alpha Competent E. coli (High Efficiency) (NEB #C2987) which has 1,000-fold higher transformation efficiency.
Highlights
  • Activity of nonspecific endonuclease I (endA1) eliminated for highest quality plasmid preparations
  • Efficient transformation of unmethylated DNA derived from PCR, cDNA and many other sources (hsdR)
  • Reduced recombination of cloned DNA (recA1)
  • Resistance to phage T1 (fhuA2)
  • Suitable for blue/white screening by α-complementation of the β-galactosidase gene
  • K12 Strain
  • DH5α™ derivative
  • Free of animal products
Reagents Supplied

The following reagents are supplied with this product:

NEB # Component Name Component # Stored at (°C) Amount Concentration
  NEB® 5-alpha Competent E. coli (Subcloning Efficiency) C2988JVIAL -80 6 x 0.4 ml
Features
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 this step is shortened.

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 this step is shortened. 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.
Application Features

Effect of DNA Purity on Transformation Efficiency and Colony Output: Effect of DNA Purity on Transformation Efficiency and Colony Output:
The total colonies which can be obtained from a single transformation reaction with NEB 5-alpha Competent E.coli (Subcloning Efficiency) are not significantly reduced when using miniprep DNA. Using 10 ng-1000 ng of clean, supercoiled pUC19 or pUC19 isolated with a commercial miniprep kit, total colonies increase with increasing DNA concentration.
* 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, a purification step, either a spin column (NEB #T1030) or phenol/chloroform extraction and ethanol precipitation should be added.
Effect of heat shock time on NEB 5-alpha competent E.coli transformation efficiency: Effect of heat shock time on NEB 5-alpha competent E.coli transformation efficiency:
50 μl of competent cells were transformed with 100 pg of pUC19 control DNA following the provided High Efficiency Transformation Protocol except heat shock time varied from 0 to 80 seconds.
Effect of DNA incubation time on NEB 5-alpha competent E.coli transformation efficiency: Effect of DNA incubation time on NEB 5-alpha competent E.coli transformation efficiency:
50 μl of competent cells were transformed with 100 pg of pUC19 control DNA following the provided High Efficiency Transformation Protocol except DNA incubation time varied from 0 to 40 minutes.
Effect of outgrowth medium on transformation efficiency: Effect of outgrowth medium on transformation efficiency:
50 μl of NEB 5-alpha competent E.coli was transformed with 100 pg of pUC19 control DNA following the provided High Efficiency Transformation Protocol with the exception of varying the outgrowth medium. NEB SOC outgrowth medium delivers the highest transformation efficiency.
NEB® 5-alpha Competent E. coli (Subcloning Efficiency) | New England Biolabs
Home Competent Cells Products NEB® 5-alpha Competent E. coli (Subcloning Efficiency)

NEB® 5-alpha Competent E. coli (Subcloning Efficiency)

Having trouble opening your tubes?  NEB Tube Opener can help!

NEB 5-alpha Competent E. coli is a derivative of the popular DH5α. It is T1 phage resistant and endA deficient for high-quality plasmid preparations. 

  • Ideal for subcloning efficiency transformations, such as plasmid transformation or routine subcloning
  • No dry ice surcharge on competent cell shipments
  • Free of animal products
  • High efficiency chemical and electrocompetent formats are also available

Featured Video

Catalog https://www.neb.com/en/# Concentration Size
C2988J Not Applicable 6 x 0.4 ml
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Notes
  • NEB 5-alpha Competent E. coli (Subcloning Efficiency) is not supplied with SOC Outgrowth Medium or pUC19 Control DNA.
Quality Control Assay
Quality Control tests are performed on each new lot of NEB product to meet the specifications designated for it. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. Further information regarding NEB product quality can be found here.
Specifications
The Specification sheet is a document that includes the storage temperature, shelf life and the specifications designated for the product. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]
Certificate of Analysis
The Certificate of Analysis (COA) is a signed document that includes the storage temperature, expiration date and quality controls for an individual lot. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]_[Lot Number]
Safety Data Sheets
Legal And Disclaimer

Products and content are covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc (NEB). The use of trademark symbols does not necessarily indicate that the name is trademarked in the country where it is being read; it indicates where the content was originally developed. The use of this product may require the buyer to obtain additional third-party intellectual property rights for certain applications. For more information, please email busdev@neb.com.

This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.

New England Biolabs (NEB) is committed to practicing ethical science – we believe it is our job as researchers to ask the important questions that when answered will help preserve our quality of life and the world that we live in. However, this research should always be done in safe and ethical manner. Learn more.

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