-
PETG Media Bottle with various capacities and 28mm PETG tamper evident cap Capacities and container codes: N1L: 1000ml N500: 500ml N100: 100ml -
Pharma vial of 100ml volume capacity with injectable stopper and crimp closure. Volume(s) : 100ml -
Pharma vial of 500ml volume capacity with injectable topper and crimp closure. Volume(s) : 500ml -
A standard biochemical reagent suitable for a variety of uses, primarily the preparation of serial dilutions. -
Based on the formulation of Dulbecco Solution ‘A’ this balanced salt solution is intended for use primarily in Tissue Culture techniques. It can be used either on its own or with the addition of Calcium and Magnesium salts (Dulbecco Solution B). -
Phosphate-buffered saline (PBS) is a buffer solution used in biological research. It is a water-based salt solution containing sodium phosphate, sodium chloride and, in some formulations, it contains potassium chloride and potassium phosphate. The osmolality and ion concentrations of the solutions match those of the human body (isotonic) and are non-toxic to most cells. This balanced salt solution is issued to meet the requirements of those tissue culture workers who use the Dulbecco Solution with and without calcium and magnesium. -
Based on the formulation of Dulbecco Solution ‘A’ this balanced salt solution with added Tween is intended for use primarily in Tissue Culture techniques. It can be used either on its own or with the addition of Calcium and Magnesium salts (Dulbecco Solution B). -
Originally intended for use in surface counting and pour plating techniques this medium can be used as a general purpose medium for the cultivation of most organisms particularly those that are less fastidious in their nutritional requirements. Can also be used as a maintenance medium for stock cultures. -
Plate Count Agar (APHA) (Standard Methods Agar, Tryptone Glucose Yeast Agar) This medium is formulated to A.P.H.A. specification and intended for use in food, dairy and water bacteriology to perform Total Viable Counts. The agar is of high gel strength and is therefore suitable for use in pour plate techniques as well as surface inoculation. -
Plate Count Agar is formulated to the A.P.H.A. specification developed by Buchbinder et al. This medium is intended for use in food, dairy and water bacteriology to perform Total Viable Counts. Tryptone and yeast extract provide the required carbon, nitrogen and vitamins. Glucose is a fermentable carbohydrate.
-
Polypropylene media tube and swab-capture cap. Tube diameter: 13mm. Dimensions with cap on: 83 x 17mm. Cap colour: Green -
-
Polypropylene media tube and swab-capture cap. Dimensions with cap on: 103 x 16mm. Cap colour: Red -
Polypropylene media tube and swab-capture cap. Tube diameter: 13mm. Dimensions with cap on: 83 x 17mm. Cap colour: Red -
Polypropylene media tube and swab-capture cap. Tube diameter: 13mm. Dimensions with cap on: 83 x 17mm. Cap colour: White -
Polypropylene media tube and swab-capture cap. Tube diameter: 13mm. Dimensions with cap on: 83 x 17mm. Cap colour: Yellow -
Polypropylene universal bottle with 30ml volume capacity and a white polystyrene cap Volume(s) : 30ml -
Polystyrene Round Base Tube with Push Cap available in 75x12mm Tube with 5mm push cap -
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 medium is recommended for the detection and enumeration of yeasts and moulds in food and dairy products. It can also be used for the cultivation of fungi although with the prolonged incubation necessary cultures may become overgrown by bacteria. The low pH (5.6) suppresses the growth of most bacteria and the low mineral content ensures good pigment production by fungi where appropriate. -
Potato dextrose agar is recommended for the detection and enumeration of yeasts and moulds in food and dairy products.It can also be used for the cultivation of fungi although with the prolonged incubation necessary cultures may become overgrown by bacteria. The low pH (5.6) suppresses the growth of most bacteria and the low mineral content ensures good pigment production by fungi where appropriate. This medium meets the requirements of the Harmonised USP/EP/JP.(1,2&3) REFERENCES (1) United States Pharmacopeial Convention. 2007. The United States pharmacopeia, 31st ed., Amended Chapters 61, 62, 111. The United States Pharmacopeial Convention, Rockville, MD. (2) Directorate for the Quality of Medicines of the Council of Europe (EDQM). 2007. The European Pharmacopoeia, Amended Chapters 2.6.12, 2.6.13, 5.1.4, Council of Europe, 67075 Strasbourg Cedex, France. (3) Japanese Pharmacopoeia. 2007. Society of Japanese Pharmacopoeia. Amended Chapters 35.1, 35.2, 7. The Minister of Health, Labor, and Welfare.
-
This medium is recommended for the detection and enumeration of yeasts and fungi in a variety of sample types. The low pH (5.6) and addition of streptomycin will ensure that the growth of most bacterial species is inhibited and the low mineral content ensures good pigment production by fungi where appropriate. -
Chromogenic Coliform Agar (CCA) Chromogenic Coliform Agar (CCA) conforms to the ISO 9308-1 guidelines for the detection, enumeration and isolation of coliforms and more specifically Escherichia coli in water samples by the membrane-filtration technique. The colonial differentiation is provided by the chromogenic substrates, Salmon-GAL and X-glucuronide. Salmon-GAL is used for the detection of β-D-galactosidase enzymatic activity. X-glucuronide is used for the detection of β-D-Glucoronidase enzymatic activity. β-D-galactosidase, expressed by all coliforms, cleaves the Salmon-GAL substrate and producing red/pink coloured colonies. Unlike other coliforms, Escherichia coli leaves both Salmon-GAL and X-glucuronide producing a violet/blue coloured colonies. Tryptophan is used to increase detection reliability by improving the indole reaction. The peptones, sodium pyruvate and sorbitol support bacterial growth and simple recovery of sub-lethal thermally injured coliforms. Sodium di-hydrogen phosphate and di-sodium hydrogen phosphate phosphate buffer the medium and sodium chloride is used to achieve osmotic balance. The selectivity is attained by the addition of Tergitol® 7 as it inhibits the growth of Gram positive bacteria. -
Primary Listeria Selective Supplement E&O Laboratories Ltd Primary Listeria Selective Supplement (LS0210) is a selective mixture used to supplement Primary Listeria Selective Agar (E&O PP7025) in order to facilitate the isolation of Listeria monocytogenes in foodstuffs and other samples. -
Primary Membrane Lactose Glucuronide Agar (mLGA) is used for the differentiation and enumeration of Escherichia coli and other coliforms through a single membrane filtration technique. The peptone and yeast extract provide the required nitrogen, carbon and vitamins. Sodium pyruvate protects injured cells enhancing recovery and growth of coliforms. Sodium lauryl sulphate is a selective agent that inhibits Gram-positive organisms. Lactose is a fermentable carbohydrate and phenol red is a pH indicator. Lactose fermentation will result in yellow colonies. X-glucuronide is a chromogenic substrate which can be cleaved by the enzyme ß-glucuronidase present in E. coli. This results in a blue colony, but in combination with lactose fermentations colonies will appear green. NB: Prepared plates stored at 28°C may show formation of surface crystals which will disappear when plates are warmed to >20°C Related Supplements :
-
Traditionally, membrane Lauryl Suphate Broth (mLSB) was used as the standard media for isolating coliforms (including E. coli) from drinking water. Primary membrane Lactose Glucuronide Agar (mLGA) is a chromogenic modification of mLSB formulation aimed at reducing costs by reducing the number of filters used per test sample and aiding in the recovery and identification of coliforms and <em,>E. coli . The medium has been modified from the mLSB formulation by the incorporation of X-glucuronide, sodium pyruvate and agar. X-glucuronide is incorporated to allow for the presumptive isolation of E. coli, sodium pyruvate aids recovery of chlorine stressed organisms and agar is incorporated to remove the need for absorbent pads. This medium is recommended for the enumeration of coliform bacteria and E. coli by a single membrane filtration technique in The Environment Agency’s - The Microbiology of Drinking Water 2009 (Part 4). -
Tryptone Bile X (TBX) - Glucuronide Agar Recent developments in culture media have given rise to the use of chromogenic substrates as a means of differentiating bacteria particularly among the coliform group of organisms. This is one such medium and has been developed as a selective medium for the isolation and enumeration of Escherichia coli in food samples. Based on Tryptone Bile Agar it incorporates the chromogenic agent X-glucuronide, which detects glucuronidase activity, the same enzyme as is detected by MUG reagent. Escherichia coli can be differentiated from other coliform organisms by the presence of glucuronidase resulting in the colonies being blue/green while the other coliforms are colourless. For information on the full technical detail as to the functionality of this medium reference should be made to the many publications available. -
Side 1: Primary UTI Chromogenic Agar This is a chromogenic medium based on CLED that has been developed to allow differentiation and presumptive identification of organisms typically found in urinary tract infections. Reduced electrolyte concentration prevents swarming of Proteus spp. A sophisticated binary chromogenic system and supplementation with tryptophan allows differentiation of enterococci (turquoise colonies), Proteus spp (clear colonies with a brown halo), Enterobacter spp (metallic blue colonies), staphylococci (white colonies), and E. coli (purple colonies). Side 2: Columbia Agar w 7% Defibrinated Horse Blood & CNA This is a selective medium for the isolation of Staphylococcus/ spp and Streptococcus spp. It is based on Columbia Agar enriched with defibrinated horse blood which promotes good colony appearance, pigment production and excellent haemolysis from beta-haemolytic streptococci. The medium is made selective by the inclusion of colistin and nalidixic acid to suppress growth of the majority of Gram-negative bacteria. -
Recent developments in culture media have given rise to the use of chromogenic substrates as a means of differentiating bacteria particularly among the coliform group of organisms. This is one such medium and has been developed with the aim of simplifying the differentiation and presumptive identification of the main organisms usually found in Urinary Tract Infections (UTI). The peptone is the source of the required nitrogen, carbon and vitamins. Based on the traditional CLED medium, to prevent the swarming of Proteus spp., two chromogens are present in the medium. One allows the detection of enterococci giving rise to blue colonies whilst the second results in purple colonies of E. coli. Phenylalanine and tryptophan are also included as indicators of tryptophan deaminase activity producing brown colonies of Proteus spp. Related Supplements : SHS500 Sterile Horse Serum 500ml
-
This is a chromogenic medium based on CLED that has been developed to allow differentiation and presumptive identification of organisms typically found in urinary tract infections. Reduced electrolyte concentration prevents swarming of Proteus spp. A sophisticated binary chromogenic system and supplementation with tryptophan allows differentiation of Enterococcus spp. (turquoise colonies), Proteus spp. (clear colonies with a brown halo), Enterobacter spp. (metallic blue colonies), Staphylococcus spp. (white colonies), and E. coli (purple colonies). -
Recent developments in culture media have given rise to the use of chromogenic substrates as a means of differentiating bacteria particularly among the coliform group of organisms. This is one such medium and has been developed with the aim of simplifying the differentiation and presumptive identification of the main organisms usually found in Urinary Tract Infections. Based on the traditional CLED Medium, to prevent the swarming of Proteus spp, two chromogens are present in the medium. One allows the detection of enterococci giving rise to blue colonies whilst the second results in purple colonies of E. coli. Phenylalanine and Tryptophan are also included as indicators of Tryptophan deaminase activity producing brown colonies of Proteus spp. This media is an opaque version to aid differentiation and presumptive identification of the bacteria isolated. -
This is a medium for the isolation and identification of Group B streptococci. The principal of the medium is based on the ability of group B streptococci to produce unique orange/red pigmented colonies when incubated anaerobically, particularly on media containing starch products. This medium is non-selective so other organisms will grow on this medium but they do not produce the characteristic pigment. -
This is a selective medium for the isolation of Pseudomonas spp. primarily in food, water and environmental samples. Pseudomonas agar base is on Kings A medium which uses magnesium and potassium salts to enhance pigment production. The gelatine peptone and acid hydrolysed casein acts as a nitrogen, vitamins, and carbon source. Magnesium chloride and potassium sulphate promotes production of pyocyanin. The medium can be made selective for P. aeruginosa by the addition of Pseudomonas CN Supplement (LS0006). Alternatively, the medium can be made selective for Pseudomonas spp. generally by the addition of Pseudomonas CFC Selective Supplement (LS0026). The presence of blue/green or brown pigmentation or fluorescence is indicative of presumptive Pseudomonas spp. It should be noted however that further testing must be carried out to confirm the full identity of the organism.
-
Pseudomonas Agar Base with 1% Glycerol, Cephalothin, Fucidin & Cetrimide (CFC) This is a selective medium for the isolation of Pseudomonas spp primarily in food, water and environmental samples. The medium uses Magnesium and Potassium salts to enhance pigment production and is made selective by the addition of CFC supplement. The presence of blue/green or brown pigmentation or fluorescence is indicative of presumptive Pseudomonas spp. It should be noted however that further testing must be carried out to confirm the full identity of the organism. -
Pseudomonas Agar Base with 1% Glycerol & CN Supplement A selective medium for the isolation of Pseudomonas aeruginosa the medium is made selective by the inclusion of Cetrimide and Naladixic Acid (CN) supplement to significantly reduce the enteric organisms particularly Proteus and Klebsiella spp. Magnesium and Potassium salts are included to enhance the production of the pigments pyocyanin and fluorescein. -
Pseudomonas CFC Selective Supplement E&O Laboratories Ltd Pseudomonas CFC Selective Supplement (LS0026) is an antibiotic supplement used to enhance the selective isolation of pseudomonads primarily from food and environmental samples.
-
E&O Laboratories Limited Pseudomonas Selective CN Supplement (LS0006) is an antibiotic supplement used to enhance the selective isolation of Pseudomonas species particularly Pseudomonas aeruginosa.
-
A selective medium for the isolation of Pseudomonas spp. primarily in food, water and environmental samples the medium is made selective by the addition of CFC supplement (cetrimide, at a concentration of 10mg/L which is said to allow the growth of all pseudomonads, cephalothin and fucidin). The presence of blue/green or brown pigmentation or fluorescence is indicative of presumptive Pseudomonas spp. It should be noted however that further testing must be carried out to confirm the full identity of the organism. -
R2A agar is used for the enumeration and cultivation of bacteria from drinking water. R2A agar developed by Reasoner and Geldreich is a low nutrient medium that can used in pour plate, spread plate, and membrane filtration methods for heterotrophic plate counts. In combination with a lower incubation temperature and longer incubation period R2A agar stimulates the growth of stressed and chlorine-tolerant bacteria. Traditionally nutritionally rich media have been used for this purpose but these media support the growth of fast-growing bacteria and may suppress slow growing or stressed bacteria found in treated water. Enzymatic digest of casein, proteose peptone, acid hydrolysate of casein and yeast extract provide the required nitrogen, carbon and vitamins. Glucose is a fermentable carbohydrate. Dipotassium hydrogen phosphate is a buffering agent. Magnesium sulphate is a source of divalent cations and sulphate. Starch and sodium pyruvate aid in the recovery of stressed organisms.
-
Traditionally, standard methods for enumeration of heterotrophic bacteria in water have used nutritionally rich media with incubation at 35°C. This may represent only a small percentage of bacteria present in the sample. R2A agar is a nutritionally reduced medium which, when combined with incubation at lower temperatures for longer time periods, results in enhanced recovery of stressed and chlorine damaged organisms from treated waters resulting in higher more realistic bacterial counts. -
R2A medium was developed to determine the bacterial count including heterotrophic bacteria in potable waters during treatment and distribution. This medium has a low nutritional content and therefore requires extended incubation times. It is recommended by the Environmental Agency, Methods for the Examination of Waters and Associated Materials, and Standard Methods for the Enumeration of Water and Wastewater. -
Rappaport Vassiliadis (R.V.) Single Component Enrichment Broth This is an alternative to Selenite and Tetrathionate broths, as a selective enrichment broth for the isolation of Salmonellae spp from food, dairy and environmental samples and is claimed by some workers to be superior to both these formulations. It can also be used in clinical bacteriology but care must be taken to ensure that only a light inoculum is used. Malachite Green and Magnesium Chloride are included in the formulation as selective agents due to their ability to inhibit most enteric organisms but allow salmonellae to multiply freely. NB: This media is not recommended for use when salmonella typhi is suspected. -
This is a selective enrichment broth for the isolation of Salmonella spp. from pharmaceutical, food, dairy and environmental samples. Malachite Green and Magnesium Chloride are included in the formulation as selective agents due to their ability to inhibit most enteric organisms whilst allowing Salmonella spp. to multiply freely. Gram +ve bacteria and most other enteric bacteria, are typically susceptible to or inhibited by Malachite Green, the high osmotic pressure and/or the low pH of the medium. It should be noted that S.typhi and S.choleraesuis are sensitive to Malachite Green and may therefore be inhibited. This medium conforms to the requirements of the Harmonised USP/EP/JP. -
Rappaport-Vassiliadis (MSRV) Medium Semi-Solid is a modification of Rappaport-Vassiliadis Soy Broth for detecting motile Salmonella spp. in faeces and food products.[1] The original research on MSRV Medium revealed a semi-solid could be used as a rapid and sensitive test for isolating motile Salmonella spp. from food products following pre-enrichment or selective enrichment.[2] The semi-solid medium allows motility to be detected as halos of turbid growth around the original point of inoculation. The peptones are to provide vitamins, nutrients and nitrogen to encourage growth of Salmonella spp. The salt maintains the osmotic balance and potassium dihydrogen phosphate is a buffer for stabilising the pH of the medium. Malachite green is included as a selective agent that inhibits Gram-positive organisms and some Gram-negative organisms. References (1) ISO 6579-1:2017. Microbiology of the food chain – Horizontal method for the detection, enumeration and serotyping of Salmonella – Part 1: Detection of Salmonella spp. (2) De Smedt J.M., Bolderdikj R., Rappold H. and Lautenschlaeger D. 1986. Rapid Salmonella Detection in Foods by Motility Enrichment on a Modified Semi-Solid Rappaport-Vassiliadis Medium. J. Food Prot. 49:510-514
-
Rappaport-Vassiliadis Soya Broth is used for the enrichment and selective isolation of Salmonella spp. This medium is a modification of the original formulation by Rappaport et al. and has been formulated to exploit the full characteristics of Salmonella spp. These characteristics include the ability to survive at relatively high osmotic pressure, to multiply at low pH values and greater resistance to malachite green. This formulation also has the correct amount of magnesium chloride as previous formulations did not take into account the volume of displacement caused by dissolving large amounts of magnesium chloride in water. This formulation has been shown to be superior to tetrathionate broth and selenite broth for the isolation of Salmonella spp. from meat products. Soya peptone provides the required carbon, nitrogen and vitamins. Potassium dihydrogen phosphate and di-potassium hydrogen phosphate act as buffers. Magnesium chloride raises the osmotic pressure in the medium. Malachite green is an inhibitory substance. NB: This formulation is very hygroscopic and will produce a slight exothermic reaction when mixed with water.
-
An osmotically controlled solution for the preparation of suspensions of food samples and for use as a diluent in dilution techniques for bacterial enumeration. The solution may also be used in the sampling of food production apparatus by the rinse and swab method. -
An osmotically controlled solution for the preparation of suspensions of food samples and for use as a diluent in dilution techniques for bacterial enumeration. The solution may also be used in the sampling of food production apparatus by the rinse and swab method. -
This is a variation on the common osmotically controlled Ringers solution, where glass beads have been added to enhance macerations in the preparation of suspensions of samples and for use as a diluent in dilution techniques for bacterial enumeration. The solution may also be used in the sampling of food production apparatus by the rinse and swab method. -
RPMI Medium for E-Test RPMI Medium is recommended for use in anti-fungal susceptibility testing of yeasts from clinical isolates using the E-Test method. The medium is based on a simple Glucose Agar with added RPMI-1640 Medium (without Sodium Bicarbonate & Phenol Red), which supplies the necessary vitamins and amino-acids, and MOPS (3-(Morpholino)propanesulfonic Acid) Buffer to maintain the medium pH during incubation. -
Sabouraud Dextrose Agar with Chloramphenicol (0.5g/L) is a selective media for the isolation of yeasts and fungi suitable for use in all areas of mycology. Sabouraud dextrose agar is a modification of a medium originally described by Sabouraud.(1) The tryptone and meat peptone provides the required nitrogen, carbon and vitamins. The high concentration of dextrose is included as an energy source. Due to the higher pH of the medium, an increased concentration of chloramphenicol is included to improve the selectivity of the media and inhibit a range of Gram-positive and Gram negative bacteria. 1. Sabouraud, R. 1892. Ann. Dermatol. Syphilol. 3:1061.
