MultiShot™ StripWell Mach1™ T1 Phage-Resistant Chemically Competent E. coli
MultiShot&trade; StripWell Mach1&trade; T1 Phage-Resistant Chemically Competent <i>E. coli</i>
Invitrogen™

MultiShot™ StripWell Mach1™ T1 Phage-Resistant Chemically Competent E. coli

MultiShot StripWell Mach1 T1R chemically competent E. coli cells are exceptionally fast-growing cloning competent cells packaged in a rack containingRead more
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Catalog number C869601
Price (USD)
1,052.00
Each
Add to cart
Price (USD)
1,052.00
Each
Add to cart

MultiShot StripWell Mach1 T1R chemically competent E. coli cells are exceptionally fast-growing cloning competent cells packaged in a rack containing 12 strips of 8 tubes for increased productivity of bacterial transformations. The Mach1 T1R strain is derived from a non-K-12, wild-type W E. coli strain (ATCC #9637) that was selected for its rapid growth rate, and genetically manipulated to possess the most useful cloning strain features.

All of our T1R strains have the tonA (also known as fhuA) deletion in their genotype that confers resistance to T1 and T5 phage. T1 bacteriophage spread rapidly and lyse E. coli hosts, which are commonly used for cloning and library construction. A resistant genotype offers added security to protect valuable clones and libraries. This is especially important for genome and sequencing centers where T1 phage infection would be catastrophic.

Accelerate cloning workflow using Mach1 T1R strain
MultiShot StripWell Mach1 T1R competent E. coli cells are fast growing chemically competent cells with a doubling time of approximately 50 minutes, with other popular strains averaging 70 minutes. Mach1-T1R colonies are clearly visible within 8 hours of plating the transformation mix (ampicillin selection), enabling you to plate and pick colonies the same day. You can also prepare plasmid DNA 4 hours after inoculating a single, overnight-grown colony in the selective media of choice (with any antibiotic). The Mach1 T1R strain is useful for many cloning applications and provides transformation efficiencies in the MultiShot StripWell format of >1 x 108 cfu/μg with plasmid DNA.

The Mach1 T1R strain was engineered to carry the tonA mutation that confers resistance to T1 and T5 phage infection. The tonA genotype offers added security to valuable clones and libraries. The Mach1 T1R strain has the lacZΔM15 genotype, allowing blue-white screening on plates containing either X-Gal or Bluo-Gal. It also carries the recA1398 mutation that helps reduce the rate of recombination while propagating plasmid DNA, the endA1 mutation that increases plasmid DNA yield and quantity, and hsdR restriction system deletion to allow genomic DNA cloning.

MultiShot StripWell Mach1 T1R Competent Cells offer:
• Transformation efficiencies in StripWell format of >1 x 108 cfu/μg plasmid DNA
tonA (fhuA) genotype to confer resistance to T1 and T5 phage
lacZ∆M15 for blue-white color screening of recombinants
hsdR mutation for efficient transformation of unmethylated DNA from PCR applications
recA1398 mutation for reduced occurrence of homologous recombination in cloned DNA
endA1 mutation for increased plasmid yield and quality

MultiShot StripWell flexible format
Each StripWell of eight connected tubes is designed with the same single-tube, single-use features as our One Shot format tubes. This format allows all steps of the transformation protocol, up to plating, to take place in the same tube, thereby saving time and reducing chance of contamination. After addition of DNA, MultiShot StripWell competent cells can be transformed by heat-shock at 42°C using a water bath, all in the same tube.

The StripWell tubes can be cut to permit transformations in a single tube, eliminating wasted aliquots of cells and avoiding freeze-thaws that can result in reduced transformation efficiency.

Benifits of the MultiShot StripWell format include:
Increased productivity—suitable for high throughput experimentation
Maximal flexibility—transform as few as 1 or as many as 96 tubes from the StripWell rack
Familiar convenience—add DNA directly to cells, heat shock, and recover in the same tube

Genotype
F φ80lacZΔM15 ΔlacX74 hsdR(rK–, mK+) ΔrecA1398 endA1 tonA

Find the strain and format that fits your needs
A variety of E. coli strains and formats of chemically competent and electrocompetent cells are available to meet transformation needs.
For high-throughput transformation choose from our collection of MultiShot comp cells or email us for custom formatting options.
We offer bacterial growth media in various formats.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Product TypeChemically Competent Cells
Contains F' EpisomeNo
Improves Plasmid QualityYes (endA1)
Cloning Methylated DNANo
Transformation Efficiency LevelHigh Efficiency (>1 x 109 cfu/μg)
Antibiotic Resistance BacterialNo
Cloning Unstable DNANot suitable for cloning unstable DNA
Blue/White ScreeningYes (lacZΔM15)
High-throughput CompatibilityHigh
Preparing Unmethylated DNANo
Reduces RecombinationYes (recA1)
Shipping ConditionDry Ice
T1 Phage - Resistant (tonA)Yes
SpeciesE. coli (wild-type W)
Format8-well Strips
Product LineMultiShot™
Quantity1 x 96 tube rack (50 μl/tube)
Unit SizeEach
Contents & Storage
• Mach1 T1 Phage-Resistant (T1R) Chemically Competent E. coli (1 x 96-stripwell plate at 50 μL/well); store at –80°C
• pUC19 DNA (1 x 50 μL at 10 pg/μL); store at –20°C
• S.O.C. Medium (2 x 15 mL); store at 4°C or room temperature

Frequently asked questions (FAQs)

I'm making a yeast genomic library and want to transform and amplify it in one of your competent cell strains. What genotype features should I look for in choosing a good strain?

We would recommend a mcr/mrr- strain, which prevents restriction of methylated eukaryotic DNA in the E. coli host. We would also recommend using a T1R strain, as T1 is a common contaminant in genomic/cDNA libraries.

Which is your fastest growing strain of competent cells?

Our Mach1-T1R competent cells grow faster than any of our common cloning strains. It has a doubling time of 54 minutes versus doubling times in excess of 70 mins for standard cloning strains, such as DH5α cells. Colonies of Mach1-T1R begin to be visible on a plate 8 hours after plating the transformation mix at 37 degrees C. It can be mini-prepped from 1.5 mL cultures in as little as 4 hours at 37 degrees C after inoculation with a single large overnight colony.

Is it possible to perform a fast transformation protocol with the MultiShot competent cells?

There are situations where either because of time or process limitations, elimination of the heat shock and recovery time post-heat shock in the transformation protocol would be desirable. Testing was performed on many of our chemically competent cells in both the MultiShot StripWell and MultiShot FlexPlate format with a shortened transformation protocol. Use of a rapid transformation protocol (add DNA, no heat shock, no recovery period, plate on warm agar) yielded up to a log lower in transformation efficiency using the control DNA. This rapid transformation protocol can be performed with expectation of lower colony counts than our standard high efficiency transformation protocol and can only be performed with plasmids that use ampicillin as their antibiotic resistance. The rapid protocol is ideal when using a liquid handling system for high-throughput transformations with high cloning efficiency. Please see the product manual for full details on this rapid transformation protocol option.

Can I use a thermal cycler or heat block to heat shock the competent cells in the MultiShot FlexPlate?

The MultiShot FlexPlate is a PCR plate and can be placed in a thermal cycler or heat block set at 42 degrees C to transform the cells by the heat shock method. The duration of the heat shock performed in these devices has yielded similar transformation efficiencies as that seen with heat shock done in a water bath.

Which E. coli strains do you offer in the MultiShot StripWell format?

We offer the following E. coli strains in the MultiShot StripWell format: TOP10, DH5alpha T1R, Mach1 T1R, Stbl3, and BL21 Star (DE3) chemically competent cells.