1.46333

Fluid Thioglycollate Medium Clear

bottle capacity 125 mL, bottle filling volume 100 mL, closure type, Red screw cap with septum and protector, pack of 10 bottles

• Synonim(y): Clear Fluid Thioglycollate Medium, Clear FTM, Clear Thioglycollate Broth, CTM
• NACRES: NA.74
• UNSPSC Code: 41106200
• Bottle capacity: 125 mL
• Bottle filling volume: 100 mL
• Feature: closure type Red screw cap with septum and protector, ready-to-use
• Agency: EP 2.6.1, JP 4.06, USP 71
• Ph: 7.1

Właściwości

• Quality Level: 300
• agency: EP 2.6.1, JP 4.06, USP 71
• sterility: sterile; autoclaved
• form: liquid (ready-to-use)
• shelf life: 12 mo.
• feature: closure type Red screw cap with septum and protector, ready-to-use
• packaging: pack of 10 bottles, single packed of (100 ml in 125 ml bottle with red screw cap and septum (10 bottles per box))
• bottle capacity: 125 mL
• bottle filling volume: 100 mL
• pH: 7.1
• application(s): cosmetics; pharmaceutical; sterility testing
• storage temp.: 2-25°C
• suitability: aerobic bacteria, anaerobic bacteria

Opis

General description

Fluid Thioglycollate Medium Clear is a universal complex medium. Thioglycollate and L-Cystine in the medium reduce the redox potential of the culture medium to create an anaerobic atmosphere. These agents also inactivate mercury and other heavy metal compounds. Resazurin indicates the reduction potential of the medium. Change of color from yellow to pink indicates an increase in oxygen concentration. Fluid Thioglycollate Medium Clear contains a reduced agar content, supplemented by a clear gelling agent, to offer the same media properties as FTM, with extra clarity.

Application

Fluid Thioglycollate Medium Clear is used for the isolation and cultivation of fastidious anaerobic as well as for aerobic microorganisms. This medium is suitable for sterility control of pharmaceutical products.

Features and Benefits

Our ready to use media provide the highest level of quality and testing confidence. They have been formulated and tested to meet the pharmacopoeia requirements. Sterility testing media and rinse solutions are manufactured in an ISO 9001, environmentally controlled production center. Each lot undergoes a stringent quality control (QC) procedure, including pH, sterility and growth promotion tests. Our manufacturing approach ensures the highest level of clarity for our media and rinsing fluids, therefore improving accuracy and significantly reducing the risk of incorrect interpretation and false results.

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Informacja o środkach bezpieczeństwa

• Klasa składowania: 12 - Non Combustible Liquids
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• wgk: WGK 1