E. coli químicamente competente One Shot™ TOP10
<i>E. coli</i> químicamente competente One Shot&trade; TOP10
Invitrogen™

E. coli químicamente competente One Shot™ TOP10

Se suministran células de E. coli químicamente competentes de One Shot™ TOP10 con una eficacia de transformación de 1 xMás información
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Número de catálogoCantidad
C40400640 reacciones
C40401011 x 50 μl
C40400321 x 50 μl
Número de catálogo C404006
Precio (CLP)
-
Cantidad:
40 reacciones
Se suministran células de E. coli químicamente competentes de One Shot™ TOP10 con una eficacia de transformación de 1 x 109 ufc/µg de ADN plasmídico que resultan ideales para la clonación y la propagación plasmídica de alta eficacia. Estas células permiten la replicación estable de plásmidos de número de copias alto y son las mismas células competentes que se incluyen en muchos de nuestros kits de clonación. Células One Shot™ TOP10:

• Maximización de la eficacia de la clonación en formato de tubo único
• Capacidades de clonación de ADN genómico mejoradas

Formato One Shot™ fácil de usar
El formato de tubo único y un solo uso permite que todos los pasos del protocolo de transformación, hasta la siembra en placa, tengan lugar en el mismo tubo, lo que permite ahorrar tiempo y evitar la contaminación.

Capacidades de clonación versátiles
Las células de E. coli de One Shot™ TOP10 son similares a las de la cepa DH10B™ y poseen las características siguientes:

• hsdR para una transformación eficaz de ADN no metilado procedente de amplificaciones de PCR
• mcrA para una transformación eficaz de ADN metilado procedente de preparaciones genómicas
• lacZΔM15 para la detección de color blanco o azul de clones recombinantes
• endA1 para preparaciones de ADN de limpiador y una mejora de los resultados en las aplicaciones secuencia abajo gracias a la eliminación de la digestión no específica por parte de Endonuclease I
• recA1 para reducir los casos de recombinación no específica en ADN clonado

Genotipo: F- mcrA Δ(mrr-hsdRMS-mcrBC) Φ80lacZΔM15 Δ lacX74 recA1 araD139 Δ(araleu)7697 galU galK rpsL (StrR) endA1 nupG

Encuentre la cepa y el formato que necesite
También ofrecemos muchas otras cepas y formatos diferentes de células químicamente competentes y células electrocompetentes para satisfacer sus necesidades específicas de transformación. Si usted requiere una transformación de alto rendimiento, elija un elemento de nuestra colección de células compuestas con formato MultiShot™.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Resistencia bacteriana a los antibióticosYes (Streptomycin)
Tramado azul/blanco
Clonación de ADN metilado
Clonación de ADN inestableNo es adecuado para clonar ADN inestable
Contiene el episoma F'Carece de episoma F'
Compatibilidad de alto rendimientoNo compatible con alto rendimiento (manual)
Mejora la calidad de los plásmidos
PlásmidoPlasmídico de alto número de copias
Preparación de ADN no metiladoNo es adecuado para preparar ADN no metilado
Línea de productosOne Shot
Tipo de productoCélula competente
Cantidad40 reacciones
Reduce la recombinación
Condiciones de envíoDry Ice
Resistente al fago T1 (tonA)No
Nivel de eficiencia de transformaciónAlta eficacia (> 10^9 ufg⁄µ g)
FormatoTubo
EspecieE. coli
Unit SizeEach
Contenido y almacenamiento
Contiene:
E. coli químicamente competente • One Shot™ TOP10: 42 viales, 50 µl cada uno
• pUC19 DNA (10 pg/µl): 2 viales, de 50 µ l cada uno
• Medio S.O.C.: 2 frascos, 6 ml cada uno

Almacenar las células competentes a - 80 °C. Almacene el producto pUC19 DNA a - 20 °C. Almacenar el medio S.O.C. a 4 °C o a temperatura ambiente.

Preguntas frecuentes

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