6.9 ± 0.2

//6.9 ± 0.2
  • Brilliant Green Agar This medium is intended for use in the isolation of Salmonellae other than Salmonella typhi. Although it can be used as a primary isolation medium it is not recommended for this purpose and is generally used for subculture from selective enrichment media. It should be noted that the medium is highly selective and therefore not suited to the isolation of Salmonella from samples where the numbers may be low. NB:  It is not recommended that this medium be used for the isolation of Salmonella typhi and Shigella spp.
  • Colorex™ MRSA is a chromogenic medium for the selective isolation of Methicillin-Resistant Staphylococcus aureus (MRSA). The medium can be used for the routine screening of clinical specimens for MRSA from a variety of sampling sites such as the nose, throat and groin. The medium incorporates a nutritious peptone base medium and a number of selective agents to inhibit most Gram-negative and Gram-positive bacteria as well as yeasts and moulds. The chromogenic detection of specific enzyme activity leads to the formation of pink/mauve colonies indicating MRSA (including low level resistant and hetero-resistant strains) following incubation at 37°C for 18-24 hours. Other organisms, if present are indicated by blue or colourless colonies. Any presumptive isolates must be confirmed using serological and/or biochemical techniques available to the laboratory. The use of this chromogenic medium does not diminish the requirement for conventional antimicrobial susceptibility tests for the confirmation of methicillin resistance. Limitations: 1. S.aureus strains that possess a low MIC to the selective agent present in the medium but are mec A negative may form colonies on the medium. 2. Some MRSA strains may form typical colonies surrounded by a matte halo. The formation of the halo serves no diagnostic function. 3. Certain methicillin-resistant coagulase-negative staphylococci (CNS) may produce characteristic colonies. In some cases differentiation may be achieved by examination of the colour of these colonies, as they may be considerably darker in colour (bluish purple to a very dark pink/magenta). 4. Certain bacterial species other than staphylococci may produce colonies with a characteristic colour.
  • Colorex™ MRSA is a chromogenic medium for the selective isolation of Methicillin-Resistant Staphylococcus aureus (MRSA). The medium can be used for the routine screening of clinical specimens for MRSA from a variety of sampling sites such as the nose, throat and groin. The medium incorporates a nutritious peptone base medium and a number of selective agents to inhibit most Gram-negative and Gram-positive bacteria as well as yeasts and moulds. The chromogenic detection of specific enzyme activity leads to the formation of pink/mauve colonies indicating MRSA (including low level resistant and hetero-resistant strains) following incubation at 37°C for 18-24 hours. Other organisms, if present are indicated by blue or colourless colonies. Any presumptive isolates must be confirmed using serological and/or biochemical techniques available to the laboratory. The use of this chromogenic medium does not diminish the requirement for conventional antimicrobial susceptibility tests for the confirmation of methicillin resistance. Limitations:
    • Staphylococcus aureus strains (Borderline resistant S. aureus (BORSA)) that possess a low MIC to the selective agent present in the medium but are mecA negative may form colonies on the medium.
    • Low inoculum levels of some mecC MRSA isolates may not form typical colonies if the incubation temperature is above 36°C.
    • Some MRSA strains may form typical colonies surrounded by a halo. The formation of the halo serves no diagnostic function.
    • Certain methicillin-resistant coagulase-negative staphylococci (CNS) may produce characteristic colonies. In some cases, differentiation may be achieved by examination of the colour of these colonies, as they may be considerably darker in colour (bluish purple to a very dark pink/magenta).
    • Certain bacterial species other than staphylococci may produce colonies with a characteristic colour. Presumptive isolates must be confirmed using serological, biochemical, or mass spectroscopy (MALDI-TOF) tests. The use of this chromogenic medium does not diminish the requirement for conventional antimicrobial susceptibility tests for the confirmation of methicillin resistance.
    • Staphylococcus aureus NCTC 12493 will fail to grow on this medium.
    • Definite identification as MRSA requires, in addition, a final identification as S. aureus.
  • This is a chromogenic medium for the isolation and presumptive identification of Staphylococcus aureus. Mauve colonies indicate Staph aureus following incubation (18 – 24 hours) at 37°C, other organisms, if not inhibited, are indicated by blue or colourless colonies. Studies have suggested that this media has a specificity and sensitivity of 99.4% and 95.5% respectively (Gaillot et al 2000).
  • Legionella Cystine Free Medium is intended for use in conjunction with Legionella CYE Medium (PP0200) as a secondary diagnostic medium for confirmation of a previously isolated organism. Although it contains Ferric Pyrophosphate and α-ketoglutarate it does not contain any L-Cysteine Hydrochloride. NB : This is a base medium only and will not sustain the growth of Legionella spp.
  • This is a selective medium for the isolation of Legionella spp is used primarily in water and environmental laboratories. The base agar contains Yeast Extract as a source of protein, Charcoal to neutralise growth-inhibiting substances and is supplemented with Ferric Pyrophosphate as a source of iron, L-cysteine hydrochloride and α-ketoglutarate to form amino acid and chelate respectively. ACES buffer is incorporated to maintain the optimal pH for growth. The medium is made selective by the addition of Glycine, Vancomycin & Polymyxin B to inhibit the majority of gram positive and gram negative organisms and Cycloheximide is also included to inhibit yeasts and fungi.
  • PP0070 Legionella BMPA Agar is a selective medium for the isolation of Legionella spp. used primarily in clinical and environmental laboratories. The medium contains yeast extract as a source of nitrogen, carbon and vitamins. Charcoal is also included to neutralise growth-inhibiting substances; ACES buffer/potassium hydroxide is added to maintain the optimal pH of 6.9 for growth of Legionella species. The medium includes iron (III) pyrophosphate as a source of iron, L-cysteine as an essential amino acid for the growth of Legionella species and α-ketoglutaric acid, which acts as a growth stimulant. The medium is made selective by the addition of cefamandole and polymyxin to inhibit most Gram-positive and Gram-negative organisms. Anisomycin is included to inhibit yeasts and fungi. PP0070 is recommended by the UK Standards for Microbiology Investigations and tested in accordance with ISO 11133:2014.
  • This is a basic medium for the cultivation of Legionella spp. It is intended primarily for use as a secondary diagnostic medium in conjunction with Legionella Cystine Free Medium (PP0201) for confirmation of a previously isolated organism. NB: This is a basal medium only and although it will sustain the growth of Legionella spp. It contains no selective supplements. It is therefore not recommended as a means of primary isolations from clinical samples.
  • This medium is recommended by BSI and ISO for the enumeration of viable organisms in milk and other dairy products. It can also be used as a general-purpose medium for the cultivation of most organisms, particularly those that are less fastidious in their nutritional requirements.
  • A selective medium for the isolation of fungi, particularly dermatophytes from clinical specimens, Mycological Agar is suitable for use in all areas of Mycology. The medium inhibits most bacteria due to the addition of Chloramphenicol which is added to reduce the risk of bacterial contamination when processing material that may be heavily contaminated particularly with Coliforms. Cycloheximide is also added to suppress the growth of yeasts and saprophytic fungi.