One Shot™ TOP10 Chemically Competent E. coli
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One Shot&trade; TOP10 Chemically Competent <i>E. coli</i>
Invitrogen™

One Shot™ TOP10 Chemically Competent E. coli

One Shot TOP10 Chemically Competent E. coli are ideal for high-efficiency cloning and plasmid DNA propagation and are provided atRead more
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Catalog NumberQuantity
C40400642 x 50 μL
C40401011 x 50 μL
C40400321 x 50 μL
Catalog number C404006
Price (KRW)
836,000
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Ends: 31-Dec-2025
879,000
Save 43,000 (5%)
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Quantity:
42 x 50 μL
Price (KRW)
836,000
線上優惠
Ends: 31-Dec-2025
879,000
Save 43,000 (5%)
Each
Add to cart

One Shot TOP10 Chemically Competent E. coli are ideal for high-efficiency cloning and plasmid DNA propagation and are provided at a transformation efficiency of 1 x 109 cfu/μg plasmid DNA. These cells allow stable replication of high-copy number plasmids and are the same competent cells that come with many of our cloning kits. TOP10 E. coli cells are genetically similar to the DH10B strain and have been reported to be more resilient to stress conditions like osmotic shock and acidic pH stress.

One Shot TOP10 cells:
• Maximize cloning efficiency in a single-tube format
• Provide enhanced genomic DNA cloning capabilities

TOP10 Chemically Competent E. coli cells carry mutations in the methylation-dependent restriction system (mcrA, mcrBC, and mrr) allowing the cloning of both prokaryotic and eukaryotic genomic DNA, as well as efficient plasmid rescue from eukaryotic genomes. Similar to other DH strains, TOP10 has the lacZΔM15 genotype, providing for the option of blue-white screening on plates containing either X-Gal or Bluo-Gal. The inclusion of recA1 and endA1 mutations increase insert stability and improve the quality of plasmid DNA prepared from minipreps.

One Shot TOP10 Chemically Competent E. coli cells offer:
• Transformation efficiencies of >1 x 109 cfu/μg
hsdR for efficient transformation of unmethylated DNA from PCR amplifications
mcrA for efficient transformation of methylated DNA from genomic preparations
lacZΔM15 for blue/white color screening of recombinant clones
endA1 for cleaner DNA preparations and better results in downstream applications due to elimination of nonspecific digestion by Endonuclease I
recA1 for reduced occurrence of nonspecific recombination in cloned DNA
• Expression from the lac promoter without IPTG

Easy-to-use One Shot format
TOP10 Chemically Competent E. coli cells are supplied in the convenient, single-reaction One Shot format. The single-tube, single-use format accomodates allows all steps of the transformation protocol, up to plating, to take place in the same tube, helping save time and prevent contamination.

Genotype
FmcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74 recA1 araD139 Δ(ara-leu)7697 galU galK λ–rpsL(StrR) endA1 nupG

Find the strain and format that fit your needs 
We offer other DH strains in chemically competent and electrocompetent cell formats.
The TOP10 strain is available in several MultiShot formats for high throughput applications.
Explore bacterial growth media formats.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Antibiotic Resistance BacterialYes (Streptomycin)
Blue/White ScreeningYes (lacZΔM15)
Cloning Methylated DNAYes (mcrA)
Cloning Unstable DNANo
Contains F' EpisomeNo
High-throughput CompatibilityLow
Improves Plasmid QualityYes (endA1)
PlasmidHigh Copy Plasmid
Preparing Unmethylated DNANo
Product LineOne Shot
Product TypeChemically Competent Cells
Quantity42 x 50 μL
Reduces RecombinationYes (recA1)
Shipping ConditionDry Ice
T1 Phage - Resistant (tonA)No
Transformation Efficiency LevelHigh Efficiency (>1 x 109 cfu/μg)
FormatTube
SpeciesE. coli (K12)
Unit SizeEach
Contents & Storage
• One Shot TOP10 Chemically Competent E. coli (42 x 50 μL)
Store Competent Cells at –80°C.

• pUC19 DNA (50 μL at 10 pg/μL)
Store pUC19 DNA at –20°C.

• S.O.C. medium (6 mL)
Store S.O.C. Medium at 4°C or room temperature.

Frequently asked questions (FAQs)

What is the difference between TOP10 and TOP10F' cells?

The only difference between TOP10 and TOP10F' cells is that the latter contain the F' episome that carries the tetracycline resistance gene and allows isolation of single-stranded DNA from vectors that have an f1 origin of replication. The F' episome also carries the lacIq repressor for inducible expression from trc, tac, and lac promoters using IPTG. TOP10F' cells require IPTG induction for blue/white screening.

I am trying to clone an insert that is supposedly pretty toxic. I used DH5? and TOP10 cells for the transformation and got no colonies on the plate. Do you have any suggestions for me?

If the insert is potentially toxic to the host cells, here are some suggestions that you can try:

- After transforming TOP10 or DH5? cells, incubate at 25-30°C instead of 37°C. This will slow down the growth and will increase the chances of cloning a potentially toxic insert.
- Try using TOP10F' cells for the transformation, but do not add IPTG to the plates. These cells carry the lacIq repressor that represses expression from the lac promoter and so allows cloning of toxic genes. Keep in mind that in the absence of IPTG, blue-white screening cannot be performed.
- Try using Stbl2 cells for the transformation.

Can I directly clone, propagate and express in BL21 without using TOP10?

It is imperative that a cloning strain such as TOP10 be used for characterization of the plasmid, propagation, and maintenance. BL21 cells are wild-type for endA and recA, which could result in poor miniprep quality and a greater chance of plasmid rearrangements due to recombination. In addition, BL21 cells contain the T7 RNA polymerase gene which is expressed at low levels even in the absence of inducer. If the gene is toxic to E. coli, plasmid instability and/or cell death can result.

I need to clone unmethylated DNA from a PCR reaction using a strain that has the hsdRMS mutation to avoid restriction after transformation. Is TOP10 suitable for my purposes?

Yes, TOP10 has the hsdRMS mutation, so this strain can be used to clone DNA from PCR reactions and other non-methylated sources. hsdRMS is a mutation in the system that E. coli uses to recognize foreign DNA. There are two parts to this system, methylation and restriction. E. coli methylate DNA at certain sequences, and if the DNA is not methylated at these sequences it will be recognized as foreign and restricted. Thus, if unmethylated DNA is transformed into E.coli that does not carry the hsdRMS genotype, it is recognized as foreign and enzymatically degraded.

Are TOP10 cells lacIq+ (plus) or lacIq- (minus)? That is, do they produce the lambda lacIq repressor protein?

TOP10 cells are lacIq- (minus). They do not have the lacIq gene and therefore do not produce the lacIq repressor protein. lacIq is most commonly found on an F' episome, and therefore is present in TOP10F', JM101, JM109, and NM522 strains.

Citations & References (3)

Citations & References
Abstract
Cloning and Characterization of a Cryptic Haloacid Dehalogenase from Burkholderia cepacia MBA4
Authors:J. Tsang and L. Sam
Journal:J Bacteriol
PubMed ID:10498712
Burkholderia cepacia MBA4 has been shown to produce a single dehalogenase batch culture.Moreover, other cryptic dehalogenases were also detected when the cells were grown in continuousculture. In this paper, we report the cloning and characterization of one of the cryptic dehalogenases inMBA4. This cryptic haloacid dehalogenase, designated Chd1, was expressed ... More
Endogenous heparan sulfate and heparin modulate bone morphogenetic protein-4 signaling and activity.
Authors:Khan SA, Nelson MS, Pan C, Gaffney PM, Gupta P,
Journal:Am J Physiol Cell Physiol
PubMed ID:18385288
Bone morphogenetic proteins (BMPs) and their endogenous antagonists are important for brain and bone development and tumor initiation and progression. Heparan sulfate (HS) proteoglycans (HSPG) modulate the activities of BMPs and their antagonists. How glycosaminoglycans (GAGs) influence BMP activity in various malignancies and in inherited abnormalities of GAG metabolism, and ... More
Methyl-CpG binding domain protein 2 represses transcription from hypermethylated pi-class glutathione S-transferase gene promoters in hepatocellular carcinoma cells.
Authors: Bakker Jila; Lin Xiaohui; Nelson William G;
Journal:J Biol Chem
PubMed ID:11960994
During the pathogenesis of human hepatocellular carcinoma (HCC), the CpG island encompassing the pi-class glutathione S-transferase gene (GSTP1) becomes hypermethylated. Repression of transcription accompanying CpG island hypermethylation has been proposed to be mediated by methyl-CpG binding domain (MBD) proteins. We report here that inhibition of transcription from hypermethylated GSTP1 promoters ... More