CMC0001
SIG10 Chemically Competent Cells
for protein expression and DNA plasmid production
About This Item
Productos recomendados
origen biológico
Escherichia coli
grado
for molecular biology
Formulario
buffered aqueous solution
modo de crecimiento
adherent or suspension
morfología
rod shaped
técnicas
microbiological culture: suitable
transformación celular
competent cell type: chemically competent
transformation efficiency: ≥1 × 109 cfu/μg
Condiciones de envío
dry ice
temp. de almacenamiento
−70°C
Categorías relacionadas
Descripción general
These cells are ideal for cloning and propagation of plasmid, cosmid, or fosmid clones and are highly efficient for routine cloning applications.
They share the most useful genetic elements of standard cloning strains like DH5α™ DH10B, JM109, TOP10, etc. and directly replace them in cloning protocols.
They are are provided in 40 μL, 80 μL and 160 μL aliquots, each being sufficient for one, two and four transformations respectively.
The cells have a transformation efficiency of >1 x 109 cfu/μg
The 96-well format are provided in aliquots of 20 μL per well and have a transformation efficiency of >1 x 108 cfu/μg.
Genotype
F- mcrA Δ(mrr-hsdRMS-mcrBC) endA1 recA1 Φ80dlacZΔM15 ΔlacX74 araD139 Δ(ara,leu)7697 galU galK rpsL nupG λ- tonA
Aplicación
Características y beneficios
- share the most useful genetic elements of standard cloning strains like DH5α™ DH10B, JM109, TOP10, etc. and directly replace them in cloning protocols.
- ensures recovery of stable and high quality plasmid DNA.
- high transformation efficiency
- provide the performance researchers need with ease of use.
- provide solutions for a wide range of applications at economical prices.
- Blue - white screening
Componentes
- SIG10 chemically competent cells
- pUC 19 transformation control DNA at 10 pg/μL
- recovery medium for cloning
Principio
This strain also carries the recA1 and endA1 mutations. The recA1 genotype provides minimized recombination and aids in plasmid stability while endA1 provides for high quality plasmid DNA preparation.
They are bacteriophage T1-resistant (tonA mutation) and also resistant to streptomycin by virtue of rpsL mutation.
Información legal
Producto relacionado
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 3
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Artículos
For best results, ligation reactions must be heat inactivated at 70ºC for 15 minutes before transformation. Alternately, the reactions may be purified.
Bacterial transformation is a process of horizontal gene transfer by which some bacteria take up foreign genetic material (naked DNA) from the environment. Bacteria that can take up free, extracellular genetic material are known as competent cells.
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