Xylose Lysine Deoxycholate Agar (XLD Agar)

Xylose Lysine Deoxycholate Agar (XLD Agar)

₹ 675.00

Brand: Micromaster

Catalog No.: DM297-100g

Quantity/Unit: 100g/Pack

Usually Shipped in: 1-2 Weeks

Qty:
Min Orderable Qty : 1 Pack
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For lab/research use only, unless otherwise specified

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Product Details

High grade Xylose-Lysine Deoxycholate Agar (XLD Agar) is supplied by Micromaster. It is available in the form of a light yellow to pink homogenous free flowing powder with a pH in the range of 7.2 to 7.6. This product should be stored between 10-30°C in a tightly closed container. Once opened, it should be properly stored, after tightly capping the bottle. Due to the hygroscopic nature of the product, there could be chances of lump formation which can be avoided by proper storage. Store in dry ventilated area protected from extremes of temperature and sources of ignition.

  •  Quantity provided: 100 g/pack

XLD Agar has been recommended for the identification of Enterobacteriaceae. XLD Agar was formulated by Taylor for the isolation and differentiation of enteric pathogens including Salmonella Typhi from other Salmonella species from foods, water and dairy products. The media formulation does not allow the overgrowth of other organisms over Salmonella and Shigella. The medium contains yeast extract, which provides nitrogen and vitamins required for growth. Though the sugars xylose, lactose and sucrose provide sources of fermentable carbohydrates, xylose is mainly incorporated into the medium since it is not fermented by Shigellae but practically by all enteric species. Sodium chloride maintains the osmotic balance of the medium. Lysine is included to differentiate the Salmonella group from the non-pathogens. Salmonellae rapidly ferment xylose and exhaust the supply. Subsequently lysine is decarboxylated by the enzyme lysine decarboxylase to form amines with reversion to an alkaline pH that mimics the Shigella reaction. To add to the differentiating ability of the formulation, an H2S indicator system, consisting of sodium thiosulphate and ferric ammonium citrate, is included for the visualization of hydrogen sulphide produced, resulting in the formation of colonies with black centers. The non-pathogenic H2S producers do not decarboxylase lysine; therefore, the acid reaction produced by them prevents the blackening of the colonies.

 

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