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Endo Agar
Cat. # Desc. Qty. Unit
221167 Endo Agar 20 SP
Intended Use:

Endo Agar is a differential and slightly selective culture medium for the detection of coliform and other enteric microorganisms.

Catalog # Description Quantity Unit
221167 Endo Agar 20 SP

BBL™ Endo Agar
Revision: 08    Revision Date: 04/01/2006   

Intended Use: «

Endo Agar is a differential and slightly selective culture medium for the detection of coliform and other enteric microorganisms.

Intended Use: » Intended Use:

Endo Agar is a differential and slightly selective culture medium for the detection of coliform and other enteric microorganisms.


Product Summary: «

The majority of the enteric plating media developed in the early years of the 20th century utilized either mixtures of bile salts or individual salts as selective agents to achieve inhibition of gram-positive species. In 1904, Endo reported the development of a culture medium for the differentiation of lactose fermenters from the nonfermenters in which no bile salts were used.1 Inhibition of gram-positive microorganisms was achieved by the sodium sulfite and basic fuchsin contained in the formulation. Endo's Fuchsin Sulphite Infusion Agar was the original name for this medium2 which is known today as Endo Agar. It was initially developed in order to facilitate the isolation and identification of the typhoid bacillus.

The original formula has been modified extensively since its introduction. The meat infusions have been replaced by a peptic digest of animal tissue. The dye composition and concentration also have been adjusted.

Over the years, Endo Agar has been an important medium in the microbiological examination of potable water and wastewater, dairy products and foods; however, the current compendia of standard methods for the examination of these materials recommend alternative media formulations.3-5

Product Summary: » Product Summary:

The majority of the enteric plating media developed in the early years of the 20th century utilized either mixtures of bile salts or individual salts as selective agents to achieve inhibition of gram-positive species. In 1904, Endo reported the development of a culture medium for the differentiation of lactose fermenters from the nonfermenters in which no bile salts were used.1 Inhibition of gram-positive microorganisms was achieved by the sodium sulfite and basic fuchsin contained in the formulation. Endo's Fuchsin Sulphite Infusion Agar was the original name for this medium2 which is known today as Endo Agar. It was initially developed in order to facilitate the isolation and identification of the typhoid bacillus.

The original formula has been modified extensively since its introduction. The meat infusions have been replaced by a peptic digest of animal tissue. The dye composition and concentration also have been adjusted.

Over the years, Endo Agar has been an important medium in the microbiological examination of potable water and wastewater, dairy products and foods; however, the current compendia of standard methods for the examination of these materials recommend alternative media formulations.3-5


User Quality Control: « User Quality Control:

See "Quality Control Procedures."

Quality control requirements must be performed in accordance with applicable local, state and/or federal regulations or accreditation requirements and your laboratory's standard Quality Control procedures. It is recommended that the user refer to pertinent CLSI (formerly NCCLS) guidance and CLIA regulations for appropriate Quality Control practices.


Reagents: « Reagents:
Endo Agar
  Approximate Formula* Per Liter Purified Water
  Dipotassium Phosphate  3.5   g
  Peptic Digest of Animal Tissue  10.0   g
  Agar  15.0   g
  Lactose  10.0   g
  Sodium Sulfite  2.5   g
  Basic Fuchsin  0.5   g
  *Adjusted and/or supplemented as required to meet performance criteria.

Warnings and Precautions: « Warnings and Precautions:

For in vitro Diagnostic Use.

If excessive moisture is observed, invert the bottom over an off-set lid and allow to air dry in order to prevent formation of a seal between the top and bottom of the plate during incubation.

Pathogenic microorganisms, including hepatitis viruses and Human Immunodeficiency Virus, may be present in clinical specimens. "Standard Precautions"6-9 and institutional guidelines should be followed in handling all items contaminated with blood and other body fluids. After use, prepared plates, specimen containers and other contaminated materials must be sterilized by autoclaving before discarding.



Information shown on this page is a short summary extracted from the QC/PI Manual, available as a PDF under the Related Documents section of this page.