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Merck

93227

Coliform ChromoSelect Agar, Modified

suitable for microbiology, NutriSelect® Plus

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NACRES:
NA.85
UNSPSC Code:
41171606
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Quality Level

form

powder

shelf life

limited shelf life, expiry date on the label

composition

agar, 10.0 g/L , bile salts, 0.80 g/L , chromogenix mixture, 0.20 g/L , dipotassium phosphate, 0.60 g/L , magnesium sulfate, 0.20 g/L , peptone, special, 8.0 g/L , potassium dihydrogen phosphate, 0.20 g/L , sodium chloride, 1.0 g/L , yeast extract, 3.0 g/L

manufacturer/tradename

NutriSelect® Plus

final pH

7.20±0.2 (25 °C)

application(s)

agriculture
bioburden testing
environmental
food and beverages
water monitoring, microbiology

storage temp.

2-8°C

suitability

Escherichia coli, coliforms

Application

Coliform ChromoSelect Agar is recommended for the simultaneous detection of Escherichia coli and thermotolerent coliforms in water, milk, dairy products and other food samples.

Preparation Note

Suspend 24 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes.

Other Notes

We offer two media types: the superior granulated GranuCult® and the cost-efficient powdered NutriSelect® culture media, depending on your needs.
The designations basic, plus, or prime are added to indicate the quality control level, from basic quality control to standard QC plus to prime for full regulatory compliance.

Legal Information

GRANUCULT is a registered trademark of Merck KGaA, Darmstadt, Germany
NutriSelect is a registered trademark of Merck KGaA, Darmstadt, Germany


Clase de almacenamiento

13 - Non Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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Frampton, E.W., et al.
Journal of Food Protection, 51, 402-402 (1988)
LeMinor, L., et al.
Ann. Inst. Pasteur, 102, 267-267 (1962)
M Kilian et al.
Acta pathologica et microbiologica Scandinavica. Section B, Microbiology, 84B(5), 245-251 (1976-10-01)
The paper describes a number of tests for the rapid detection of glycosidases including alpha-glucosidase, beta-glucosidase, beta-glucuronidase, beta-xylosidase and alpha-fucosidase. The methods use heavy suspensions of viable but non-multiplying bacteria in a buffered solution of a chromogenic substrate. The results