Competent Cell Sampler
Competent Cell Sampler
Invitrogen™

Competent Cell Sampler

The Competent Cell Sampler Kit contains a pair of four different strains of chemically competent E. coli cells in OneRead more
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Catalog number A10469
Price (USD)
218.00
Each
Add to cart
Price (USD)
218.00
Each
Add to cart

The Competent Cell Sampler Kit contains a pair of four different strains of chemically competent E. coli cells in One Shot format. Each single-use vial of cells is ready to use, with no extra pipetting steps or freeze-thaw cycles that reduce transformation efficiency. Use this kit to evaluate which strains best suit the different types of DNA used in your lab.

One Shot Mach1 T1 Chemically Competent E. coli
One Shot Mach1 T1 Chemically Competent E. coli cells are phage resistant and have a faster doubling time (∼50 minutes) than other popular E. coli cells. As a result, Mach1-T1R colonies are clearly visible within eight hours of plating transformation on ampicillin selection plates. From an overnight colony, minipreps can be performed after four hours of growth. The Mach1-T1R strain is derived from a non-K-12, wild-type W E. coli strain that has high growth speed and has been genetically manipulated to possess the most useful cloning strain features.

Mach1-T1R competent E. coli cells come in One Shot format (Cat. No. C862003) or MultiShot StripWell and FlexPlate formats for high throughput applications (Cat. No. C869601 and C8681201).

One Shot OmniMAX2 T1R Chemically Competent E. coli
The One Shot OmniMAX2 T1R Chemically Competent E. coli strain is a versatile phage-resistant strain, perfect to use in all cloning applications, including Gateway technology, TOPO PCR cloning, and cDNA and gDNA library construction. It offers the highest transformation efficiency in a chemically competent One Shot format with 5 x 109 transformants/μg plasmid DNA. The ccdA gene present on the F´ episome, carried by OmniMAX 2-T1R, is deleted, allowing negative selection of Gateway vectors since the strain is sensitive to the ccdB gene product.

OmniMAX 2-T1R cells are offered in our One Shot format (Cat. No. C854003) or MultiShot FlexPlate format for high throughput applications (Cat. No. C8581201).

One Shot Stbl3 Chemically Competent E. coli
One Shot Stbl3 Chemically Competent E. coli are designed for cloning direct repeats found in lentiviral expression vectors as these cells reduce the frequency of homologous recombination of direct repeats found in lentiviral or retroviral vectors. Stbl3 had been essential for many applications, including genome editing CRISPR workflows or vaccine development. The DNA yield from Stbl3 cells is often >10-fold higher than standard cloning strains.

Stbl3 chemically competent cells are available in One Shot format (Cat. No. C737303) or MultiShot StripWell and FlexPlate formats (Cat. No. C739601 and C7381201) for high throughput applications.

One Shot TOP10 Chemically Competent E. coli
One Shot TOP10 Chemically Competent E. coli are one of the most popular competent cell strains and are perfect for a broad range of cloning applications. They are included with many of our cloning and expression kits like TOPO and Gateway cloning kits and complement our GeneArt Gene Synthesis Services.

One Shot TOP10 competent E. coli have a transformation efficiency of 1 x 109 cfu/μg supercoiled DNA and are ideal for high-efficiency cloning and plasmid propagation. They allow stable replication of high-copy number plasmids.

TOP10 chemically competent cells are available in the One Shot format (Cat. No. C404003) or MultiShot StripWell and FlexPlate formats (Cat. No. C409601 and C4081201) for high throughput applications. TOP10 cells are also available for transformation using electroporation (Cat. No. C404050).

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Bacterial or Yeast StrainMach1, OmniMAX2, TOP10, Stbl3
FormatTube
Concentration1 x 109 cells/mL
SpeciesE. coli
Efficiency>1 x 109
Product LineOne Shot™
Product TypeChemically Competent Cells
Quantity8 x 50 μL
Shipping ConditionDry Ice
Unit SizeEach
Contents & Storage
• Two transformations each four strains chemically competent cells in One Shot format

Store at –80°C.

Frequently asked questions (FAQs)

How do you recommend that I prepare my DNA for successful electroporation of E. coli?

For best results, DNA used in electroporation must have a very low ionic strength and a high resistance. A high-salt DNA sample may be purified by either ethanol precipitation or dialysis.

The following suggested protocols are for ligation reactions of 20ul. The volumes may be adjusted to suit the amount being prepared.

Purifying DNA by Precipitation: Add 5 to 10 ug of tRNA to a 20ul ligation reaction. Adjust the solution to 2.5 M in ammonium acetate using a 7.5 M ammonium acetate stock solution. Mix well. Add two volumes of 100 % ethanol. Centrifuge at 12,000 x g for 15 min at 4C. Remove the supernatant with a micropipet. Wash the pellet with 60ul of 70% ethanol. Centrifuge at 12,000 x g for 15 min at room temperature. Remove the supernatant with a micropipet. Air dry the pellet. Resuspend the DNA in 0.5X TE buffer [5 mM Tris-HCl, 0.5 mM EDTA (pH 7.5)] to a concentration of 10 ng/ul of DNA. Use 1 ul per transformation of 20 ul of cell suspension.

Purifying DNA by Microdialysis: Float a Millipore filter, type VS 0.025 um, on a pool of 0.5X TE buffer (or 10% glycerol) in a small plastic container. Place 20ul of the DNA solution as a drop on top of the filter. Incubate at room temperature for several hours. Withdraw the DNA drop from the filter and place it in a polypropylene microcentrifuge tube. Use 1ul of this DNA for each electrotransformation reaction.

When should DMSO, formamide, glycerol and other cosolvents be used in PCR?

Cosolvents may be used when there is a failure of amplification, either because the template contains stable hairpin-loops or the region of amplification is GC-rich. Keep in mind that all of these cosolvents have the effect of lowering enzyme activity, which will decrease amplification yield. For more information see P Landre et al (1995). The use of co-solvents to enhance amplification by the polymerase chain reaction. In: PCR Strategies, edited by MA Innis, DH Gelfand, JJ Sninsky. Academic Press, San Diego, CA, pp. 3-16.

Additionally, when amplifying very long PCR fragments (greater than 5 kb) the use of cosolvents is often recommended to help compensate for the increased melting temperature of these fragments.

Find additional tips, troubleshooting help, and resources within our PCR and cDNA Synthesis Support Center.