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MilliporeSigma
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Documentos clave

EC11303

Sigma-Aldrich

Escherichia coli

Strain B, lyophilized cells

Sinónimos:

E. coli

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10 G
$415.00
25 G
$835.00

$415.00

Fecha estimada de envío12 de mayo de 2025DesdeMILWAUKEE

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10 G
$415.00
25 G
$835.00

About This Item

Número MDL:
MFCD00131026
Código UNSPSC:
12352204
NACRES:
NA.83

$415.00

Fecha estimada de envío12 de mayo de 2025DesdeMILWAUKEE

Nivel de calidad

200

esterilidad

non-sterile (not processed or packaged aseptically)

Formulario

lyophilized cells

idoneidad

not intended for starter culture

temp. de almacenamiento

−20°C

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Descripción general

Escherichia coli is a non-pathogenic, facultative anaerobic flora present in the intestine of human.[1] It belongs to the genus, Escherichia, which consists of motile gram-negative bacilli.[1]

Aplicación

Escherichia coli has been used:
  • in the isolation of DNA from lyophilized cell[2]
  • in the preparation of crude cell lysate for developing scalable purification method for recombinant protein A[3]
  • as test proteome for comparative electrophoresis[4]

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000427390
0000427390
0000324914
0000305774
0000324914

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Marta Pacheco et al.
Mikrochimica acta, 189(5), 194-194 (2022-04-16)
Janus micromotors encapsulating transition metal dichalcogenides (TMDs) and modified with a rhodamine (RhO)-labeled affinity peptide (RhO-NFMESLPRLGMH) are used here for Salmonella enterica endotoxin detection. The OFF-ON strategy relies on the specific binding of the peptide with the TMDs to induce
Diarrheagenic Escherichia coli
Nataro JP and Kaper JB
Clinical Microbiology Reviews, 11(1), 142-201 (1998)
Horizontal comparative fluorescence two-dimensional gel electrophoresis for improved spot coordinate detection
Hanneken M, et al.
Electrophoresis, 35(8), 1118-1121 (2014)
Severe atopic dermatitis is associated with a high burden of environmental Staphylococcus aureus
Leung AD, et al.
Clinical and Experimental Allergy, 38(5), 789-793 (2008)
Accelerated recombinant protein purification process development: Automated, robotics-based integration of chromatographic purification and analysis
Londo T, et al.
Journal of Chromatography A, 798(1), 73-82 (1998)
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Questions

1–2 of 2 Questions  

  1. Could you provide the reconstitution method and concentration for product EC11303 under the brand SIGMA?

    1 answer

    1. The cells in this product are expected to be viable and may grow in culture, but it's important to note that the product is not intended for culture use. The material is not handled aseptically during manufacturing, so it is likely that other organisms would be present. The main purpose of this product is to serve as a biomass, specifically for the extraction of biomolecules such as DNA and lipids. It's important to understand that there is no guarantee of viability or purity. If the end user wishes to reconstitute the product for culture, they should add 0.3 to 0.4 ml of suitable liquid medium/broth to the freeze-dried material and mix it well. Then, they should transfer the total mixture to a culture tube or plate containing 5 - 6 mL medium/broth. It's worth noting that there is no cell count estimate available for this product.

      Helpful?

  2. What is the method of reconstitution for this product and what is the concentration?

    1 answer

    1. These cells are expected to be viable and may grow in culture. However, the product is not intended for culture use. The material is not handled aseptically during manufacturing, therefore other organisms would likely be present. The product is intended to serve as a biomass, i.e., for the extraction of biomolecules such as DNA and lipids. There is no guarantee of viability or purity. Should the end user wish to reconstitute the product for culture, add to the freeze-dried material 0.3 to 0.4 ml of suitable liquid medium/broth and mix well. Transfer the total mixture to a culture tube or plate containing 5 - 6 mL medium/broth. There is no cell count estimate available.

      Helpful?

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