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Competent Cells: IG® Ultra-High Efficiency Electrocompetent E. coli Cells

IG® Ultra-High Efficiency Electrocompetent E. coli Cells

 

Intact Genomics (IG®, ig®) offers the largest collections of high-quality competent cells on the market.

Originally founded as a BAC cloning company, Intact Genomics developed deep expertise in producing ultra-high-efficiency competent cells to enable transformation of very large plasmids (~300 kb) into E. coli. Over the years, this expertise—combined with continuous process optimization—has allowed us to consistently deliver exceptionally high transformation efficiencies and reliable performance.

Combining our scientists’ expertise and craftsmanship with state-of-the-art equipment, advanced protocols, and rigorous quality control standards, our competent cells provide the following advantages:

  • Exceptional Transformation Efficiency – Up to 10–100× higher than other leading brands.
  • Consistent Quality – Manufactured under an ISO 13485:2016-certified quality management system to ensure reliable lot-to-lot performance.
  • Competitive Pricing– High-performance products at affordable prices to help maximize your research budget.
  • Flexible Formats and Custom Services – We offer a broader range of formats than competitors, including tubes (multiple aliquot sizes), 96- and 384-well plates, and strip tubes. We also provide custom competent cell services tailored to your specific needs.

Application

Product 

Specialization

Efficiency

Routine Cloning

ig® 5-alpha Electrocompetent Cells

Routine cloning and sub-cloning, library construction (DNA <10 kb)

≥2.0 × 1010

ig® 10B Electrocompetent Cells

Routine cloning and sub-cloning, library preparation including large DNA >10 kb

≥5.0 × 1010

ig® XL1 Blue Max Electrocompetent Cells

Stable plasmid propagation with blue/white screening

≥5.0 × 1010

HB101 Electrocompetent Cells

Stable plasmid maintenance

≥5.0 × 1010

Specialized Cloning

igMax™ DH10B Electrocompetent Cells

Difficult large DNA fragment cloning, BAC library construction

≥5.0 × 1010

IG® Recombineering Electrocompetent Cells

Homologous recombination, DNA, plasmid, and BAC engineering

≥1.0 × 1010

ig® Stable 2 Electrocompetent E. coli Cells

Cloning direct repeat sequences (unstable DNA)

≥2.0 × 109

ig® ccdB Resist™ Electrocompetent E. coli Cells

Propagation of plasmids containing the ccdB gene

≥1.0 × 1010

Staphylococcus aureus (S. aureus) RN4220 ElectroCompetent Cells

A gateway strain to enable DNA manipulation in Staphylococcus aureus

≥1 × 105

Protein Expression

IG® Autoinduction DE3 ElectroCompetent Cells

Optimized for autoinduction of protein expression

≥1.0 × 1010

BL21(DE3) Electrocompetent Cells

Routine T7 protein expression

≥1.0 × 1010

BL21(DE3)pLysS ElectroCompetent Cells

Routine non-T7 protein expression

≥1.0 × 1010

IG® C41(DE3) Electrocompetent Cells

Improved expression of toxic proteins

≥1.0 × 1010

IG® C41(DE3)pLysS Electrocompetent Cells

Improved expression of toxic proteins with suppressed basal expression

≥1.0 × 109

IG® C43(DE3) Electrocompetent Cells

Most tolerant of toxic proteins

≥1.0 × 1010

IG® C43(DE3)pLysS Electrocompetent Cells

Most tolerant of toxic proteins with suppressed basal expression

≥5.0 × 109

Phage Display

TG1 Phage Display Electrocompetent Cells

Antibody phage display with amber suppressor

≥4.0 × 1010

SS320 Phage Display Electrocompetent Cells

Antibody phage display

≥5.0 × 1010

ER2738 Phage Display ElectroCompetent Cells

Peptide phage display with amber suppressor

≥4.0 × 1010

Medium

IG® Recovery Medium

Superior formulation for all competent cell transformations

High-efficiency

IG® Autoinduction Medium

Promotes high-yield growth of E. coli and high-level expression of T7 promoter-regulated recombinant proteins

High-efficiency

 

Custom Formats, Custom Package Sizes and Bulk Pricing Are Available Upon Request

 

SS320 Phage Display Electrocompetent Cells

Intact Genomics SS320 (MC1061F\’) phage display electrocompetent cells are suitable for protein expression, general cloning, blue/white screening, M13 phage work and phage display protein expression.

Intact Genomics

Catalogue No.DescriptionPack SizePriceQty
  • Change to:
IG-1173-12SS320 Phage Display Electrocompetent Cells6x50µl �265.64 Quantity
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IG-1173-24SS320 Phage Display Electrocompetent Cells12x50µl �425.72 Quantity
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IG-1274-24SS320 Phage Display Electrocompetent Cells6x100µl �363.08 Quantity
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IG-1274-48SS320 Phage Display Electrocompetent Cells12x100µl �522.00 Quantity
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SS320 Phage Display Electrocompetent Cells

 

Intact Genomics SS320 (MC1061F\’) phage display electrocompetent cells are suitable for protein expression, general cloning, blue/white screening, M13 phage work and phage display protein expression.


Product Description

Specifications

Competent cell type: ElectroCompetent
Species: E. coli
Format: Tubes
Transformation efficiency: ≥ 5 x 1010 cfu/µg pUC19 DNA
Blue/white screening: Yes
Shipping condition: Dry ice

Reagents Needed for One Reaction

SS320 phage display electrocompetent cells: 25 µl
DNA (or pUC19 Control, 10 pg/µl): 1 µl
Recovery medium: 1 ml

Storage

SS320 phage display electrocompetent cells: -80 ºC
pUC19 control DNA: -20 ºC
Recovery medium: 4ºC

Genomic Features

Intact Genomics SS320 phage display electrocompetent cells have the following features:

  • >5 x 1010cfu/µg efficiency with electroporation.
  • Non-amber suppressor strain (sometimes called MC1061F\’)

Genotype

F'[proAB lacIq lacZΔM15 Tn10 (tetr)] hsdR mcrA0 araD139 Δ(araA-leu)7697 ΔlacX74 spoT1 galK λe14- galE rpsL thi

Quality Control

Transformation efficiency is tested by using the pUC19 control DNA supplied with the kit and using the protocol given below. Transformation efficiency should be >5 x 1010 CFU/µg pUC19 DNA. Untransformed cells are tested for appropriate antibiotic sensitivity.

General Guidelines

Follow these guidelines when using Intact Genomics SS320 phage display electrocompetent cells:

  • Handle competent cells gently as they are highly sensitive to changes in temperature or mechanical lysis caused by pipetting.
  • Thaw competent cells on ice and transform cells immediately following thawing. After adding DNA, mix by tapping the tube gently. Do not mix cells by pipetting or vortexing.

Note: A high-voltage electroporation apparatus such as Bio-Rad Gene Pulser II #165-2105, capable of generating field strengths of 16 kV/cm is required. 

 

Calculation of Transformation Efficiency
Transformation Efficiency (TE) is defined as the number of colony forming units (cfu) produced by transforming 1µg of plasmid into a given volume of competent cells.

TE = Colonies/µg/Dilution

Transform 1 µl of (10 pg/µl) pUC19 control plasmid into 50 µl of cells, add 950 µl of Recovery Medium. Dilute 10 µl of this in 990 µl of Recovery Medium and plate 50 µl. Count the colonies on the plate the next day. If you count 100 colonies, the TE is calculated as follows:

Colonies = 100
µg of DNA = 0.00001
Dilution = 50/1000 x 10/1000 = 0.0005
TE = 100/.00001/.0005 = 2.0×10101173-12 1173-24 1274-24 1274-48

 

Protocol

 

Use this procedure to transform Intact Genomics SS320 phage display electrocompetent cells. Do not use these cells for chemical transformation.

1. Place sterile cuvettes and microcentrifuge tubes on ice.
2. Remove competent cells from the -80 °C freezer and thaw completely on wet ice (10-15 minutes).
3. Aliquot 1 µl (1 pg-10 ng) of DNA to the chilled microcentrifuge tubes on ice.
4. When the cells are thawed, add 25 μl of cells to each DNA tube on ice and mix gently by tapping 4-5 times. For the pUC19 control, add 1 µl of (10 pg/µl) DNA to the 25 µl of cells on ice. Mix well by tapping. Do not pipette up and down or vortex to mix, this can harm cells and decrease transformation efficiency.
5. Pipette 26 µl of the cell/DNA mixture into a chilled electroporation cuvette without introducing bubbles. Quickly flick the cuvette downward with your wrist to deposit the cells across the bottom of the well and then electroporate.
6. Immediately add 974 µl of Recovery Medium or any other medium of choice to the cuvette, pipette up and down three times to re-suspend the cells. Transfer the cells and Recovery Medium to a culture tube.
7. Incubate tubes at 37 °C for 1 hour at 210 rpm.
8. Dilute the cells as appropriate then spread 20-200 μl cells onto a pre-warmed selective plate. For the pUC19 control, plate 50 μl of diluted transformants onto an LB plate containing 100 μg/ml ampicillin. Use sterilized spreader or autoclaved ColiRoller™ plating beads to spread evenly.
9. Incubate the plates overnight at 37 °C.

 

Downloads

Manual – SS320 Phage Display Electrocompetent Cells

MSDS – SS320 Phage Display Electrocompetent Cells


 

 

If you cannot find the answer to your problem then please contact us or telephone +44 (0)1954 210 200