2-30°C
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A pre-enrichment medium designed to help sub-lethally damaged Salmonella spp. recover before introducing them into a selective medium. This non-selective, nutritious medium is free from inhibitors and is well buffered to maintain the pH at 7.0 for the incubation period according to ISO 6579 (2002). -
The principle use for this product is in the testing of disinfectants and antiseptics. In 1989, the European Committee for Standardisation (CEN) set up a technical committee to produce harmonised test methods for disinfectants and antiseptics. The CEN standards provide a useful basis for disinfectant validation, and although alternative methods could be used for assessing disinfectant efficacy, following the same basic methods allows not only direct comparison between products but also comparison across various different laboratories. The adaptability of the methods - numerous validation studies based on the CEN methods have been accepted by both the European and US regulatory authorities - allows end- users to customise the methods to their specific requirements. Lecithin and polysorbate 80 (Tween 80) inactivate surface disinfectants (lecithin neutralises quaternary ammonium compounds and Tween 80 neutralises phenols, formalin, hexachlorophene and in combination with the lecithin ethanol). L-histidine, in combination with lecithin and Tween 80, neutralises aldehydes and formaldehyde generating agents. Sodium thiosulphate neutralises iodine and chlorine. -
For in vitro diagnostic use. BM0650 Deionised Water is used as a diluent for, where required, the preparation of clinical specimens and microbiological samples, the dilution of microorganisms and reconstitution of lyophilised antibiotic supplements during culture media preparation. Deionised Water is purified water that can be used as a general-purpose diluent in many areas of the laboratory. It may be used for creating 0.5 McFarland suspensions of bacterial isolates for identification tests or processing clinical specimens or industrial samples prior to microbiological examination. -
For in vitro diagnostic use. BM1682 Faecal Transport Solution is recommended for the transport of clinical specimens, especially those associated with enteric pathogens (1). This formulation allows for transport at chilled or ambient temperatures.
BM1682 Faecal Transport Solution is a modified Cary Blair Transport Medium (2), designed for the transportation and preservation of clinical specimens, primarily stool and rectal swabs. The product is designed to maintain the viability of enteric bacterial pathogens during transport and subsequent storage at chilled or ambient temperatures.
Faecal Transport Solution is an isotonic, buffered, and nonnutritive medium with a carefully balanced composition. It includes agar to help reduce oxygen diffusion, sodium thioglycolate to impede oxidation, and disodium phosphate to help maintain pH. The relatively high pH of the medium helps to minimises overgrowth of non-target organisms and prevent acid formation in the specimen. References1. CLSI M40-A2. (2014). Quality control of microbiological transport systems; Approved standard – _second edition. CLSI document M40-A2. Wayne, PA: Clinical and Laboratory Standards Institute. 2. Cary, S.G. and Blair, E.B. (1964). New Transport Medium for Shipment of Clinical Specimens. J. Bact, 88:96-98.
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Glucose agar allows for the detection of glucose fermentation (with or without gas production) as an identification test for Enterobacteriaceae (ISO 21528) and B.cereus (ISO 7932). It is further enriched by the addition of Yeast Extract. Bromocresol Purple is also included and acts as an indicator of glucose fermentation. -
For in vitro diagnostic use only. SW0005-M055-3 Strep B Swab Kit contains Lim Broth, a nutritious medium for the enrichment and transport of Group B streptococci along with a sterile swab suitable for collection of patient samples. The product may be used to preserve, transport, and enrich Group B streptococci that may be present in samples obtained from patients by use of the swab. Each pack also contains a sterile swab in an individual peel-pouch. The swab has a polystyrene shaft with a small viscose tip. The shaft has a breakpoint 78mm from the tip allowing the shortened swab to engage in the shaft capture device in the lid and ensure that the swab is removed from the tube when the cap is unscrewed. Lim broth is a nutritious, selective broth utilising the base formulation developed by Todd and Hewitt (1) for the enrichment of Group B streptococci. It is intended as a selective, enrichment broth for Streptococcus agalactiae that may be present is specimens. The device is primarily intended for use in screening pregnant women for the presence of S. agalactiae, which poses a significant risk of infection in new-born infants that may result in serious illness or death. -
Letheen Broth with Neutraliser and 1% Tween 80 is primarily intended for use in assessing the bactericidal activity of quaternary ammonium compounds and determining the phenol coefficient of cationic surfactants. It can also be used in environmental testing, particularly in areas subjected to surface disinfection. Lecithin and polysorbate 80 (Tween 80) inactivate surface disinfectants (lecithin neutralises quaternary ammonium compounds and Tween 80 neutralises phenols, formalin, hexachlorophene and in combination with the lecithin ethanol).
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This is an egg-based medium for the isolation and presumptive identification of Mycobacterium spp., particularly Mycobacterium tuberculosis, from clinical samples. Based on the original formulation of Lowenstein that was subsequently modified by Jensen, the medium contains glycerol and egg which provide the required protein and fatty acids. The coagulation of the egg albumin during preparation also provides a solid surface for inoculation purposes. Malachite green is incorporated into the medium to inhibit contaminating organisms other than the mycobacteria that may still be present in the specimen after decontamination. Lowenstein Jensen Medium slopes should be inoculated with pre-treated specimens and incubated at 35-37°C for 8 weeks in 5-10% CO2. Container caps should be left loose for the first week of incubation to allow for circulation of the carbon dioxide as this will help to stimulate growth. Caps should then be tightened to prevent any dehydration of the medium -
Lowenstein Jensen Pyruvate Medium is an egg-based medium for the cultivation of Mycobacterium spp., particularly Mycobacterium bovis. Lowenstein Jensen Pyruvate Medium is based on the original formulation of Löwenstein that was later modified by Jensen. It differs from Lowenstein Jensen Medium (BM0200) in that sodium pyruvate has replaced the glycerol, which has been demonstrated to be inhibitory to some species, particularly M. bovis. Lowenstein Jensen Pyruvate Medium can be used for the diagnosis of mycobacterial infections, testing antibiotic susceptibility of isolates, and differentiating different species of Mycobacterium (by colony morphology, growth rate, biochemical characteristics, and microscopy). It is recommended by Public Health England as a standard media for the investigation of specimens for Mycobacterium species. The coagulation of the egg albumin during preparation provides a solid surface for inoculation purposes. L-Asparagine and soluble starch are sources of nitrogen and vitamins. Potassium di-hydrogen phosphate and magnesium sulphate enhance organism growth and act as buffers. Sodium pyruvate is added to serve as a carbon source in place of glycerol. The egg mixture also provides essential fatty acids and protein to support the growth of mycobacteria. Malachite green is incorporated into the medium to exert an inhibitory effect on organisms other than mycobacteria.
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Maximum Recovery Diluent (Peptone/ Saline Diluent) An osmotically controlled solution for the preparations of suspensions of food samples and for use as a diluent in dilution techniques for bacterial enumeration. The presence of a low level peptone lessens the physiological shock normally experienced by bacterial cells when they are introduced to a diluent such as Ringers Solution. The level of peptone is such that multiplication of the organisms is not possible in the time in which the sample will be present in the diluent. -
This is a non-nutrient medium based on Page’s Amoeba Saline, a buffered salt solution, solidified with 1.5% Agar.
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Saline (0.45%) is suitable for use in preparation of food samples and/or as a rinse fluid during examination of equipment etc. prior to culture. It can also be used as a general purpose diluent in many areas of the laboratory.
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Saline (0.85%) is suitable for use in preparation of food samples and/or as a rinse fluid during examination of equipment etc. prior to culture. It can also be used as a general purpose diluent in many areas of the laboratory. -
Saline (0.9%) is suitable for use in preparation of food samples and/or as a rinse fluid during examination of equipment etc. prior to culture. It can also be used as a general purpose diluent in many areas of the laboratory. -
This is an aqueous solution of Sodium Hydroxide (2%) with Phenol Red Indicator suitable for use in the digestion of Sputum samples prior to culture of the samples for Mycobacterium spp. It is generally used in conjunction with Sputum Neutralising Buffer (BM1324). -
Sodium Hydroxide (4%) with Phenol Red is a reagent used in the digestion and decontamination of sputum samples prior to culture for mycobacteria. Most clinical specimens submitted for acid-fast bacilli isolation are contaminated with more quickly developing commensal microbial flora. Additionally, acid-fast bacilli may be retained in respiratory secretions and not released for culture until the material is liquefied. Respiratory specimens, such as sputum, contain mucin which may trap microorganisms. Decontamination and digestion of the mucous components kills contaminating normal flora and allows slower growing mycobacteria to grow. Timely neutralization prevents potential loss of mycobacteria caused by high pH levels of decontaminants, resulting in the preservation of more viable organisms. Phenol red is used to indicate changes in pH. BM1320 is recommended by the UK Standards for Microbiology Investigations as part of their decontamination/digestion protocol; it is generally used in conjunction with Sputum Neutralising Buffer without Phenol Red (BM1324). -
This is a sterile aqueous solution of Potassium di-hydrogen phosphate (16.0 % w/v) with Phenol Red Indicator suitable for use in the neutralisation following the digestion of sputum with Sodium hydroxide prior to culture. It is generally used in conjunction with BM1322 Sodium hydroxide 4%. -
This is a sterile aqueous solution of Potassium Di-Hydrogen Ortho-phosphate (16.0 % w/v) suitable for use in the neutralisation following the digestion of Sputum with Sodium Hydroxide prior to culture. It is generally used in conjunction with Sodium Hydroxide 4% with Phenol Red Indicator 0.2%. -
This buffer is intended primarily for use as a neutralising agent following treatment with alkaline compounds during the decontamination and homogenisation process of Sputum specimens prior to inoculation onto appropriate culture media for the isolation of Mycobacterium spp. -
This is a general-purpose complex medium for cultivation and isolation of fastidious bacteria, yeasts and moulds. The formulation is based on the United States Pharmacopoeia (USP Medium II) and European Pharmacopoeia (EP Medium B). The medium can be incubated under aerobic or anaerobic conditions for sterility testing, air sampling and other areas of bacteriological investigation. This product is wrapped in barrier film to allow for use in Vaporised Hydrogen peroxide sterilisation systems. This particular product is triple wrapped and terminally sterilised by Gamma irradiation. Dose Range: 8.0 kGy - 15.0kGy -
This is a general-purpose complex medium for cultivation and isolation of fastidious bacteria, yeasts and moulds. The formulation is based on the United States Pharmacopoeia (USP Medium II) and European Pharmacopoeia (EP Medium B). Lecithin and Polysorbate 80 (Tween 80) are added to inactivate surface disinfectants (Lecithin neutralises quaternary ammonium compounds and Tween 80 neutralises phenols, formalin, hexachlorophene and in combination with the Lecithin ethanol). The medium can be incubated under aerobic or anaerobic conditions for sterility testing, air sampling and other areas of bacteriological investigation. This product is wrapped in barrier film to allow for use in Vaporised Hydrogen peroxide sterilisation systems. This particular product is triple wrapped and terminally sterilised by Gamma irradiation. Dose Range: 8.0 kGy - 15.0kGy -
This is a general-purpose complex medium for the cultivation and isolation of aerobic and anaerobic microorganisms. The base medium, Tryptone Soya Agar (Soybean-Casein Digest agar), conforms to the Harmonized United States Pharmacopoeia (USP), European Pharmacopoeia (EP), and Japanese Pharmacopoeia (JP). Histidine and Sodium Thiosulphate are added to inactivate surface disinfectants (Lecithin neutralises quaternary ammonium compounds, Tween 80 and Histidine neutralises phenols, formalin, hexachlorophene and, in combination with the Lecithin, ethanol and Sodium Thiosulphate inactivates mercurials, halogens and aldehydes). The medium can be incubated under aerobic or anaerobic conditions for sterility testing, air sampling and other areas of bacteriological investigation. This product is wrapped in barrier film to allow for use in Vaporised Hydrogen peroxide sterilisation systems. This particular product is triple wrapped and terminally sterilised by Gamma irradiation. Dose Range: 8.0 kGy - 15.0kGy