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UNSPSC Code:
41106225
NACRES:
NA.72
Bottle capacity:
1000 mL
Bottle filling volume:
900 mL
Feature:
closure type White screw cap with septum and protector, ready-to-use
Agency:
EP, JP (4.06), USP
material
glass bottle
agency
EP, JP (4.06), USP
sterility
sterile; autoclaved (tested for 14 days at 30-35°C)
sterilization compatibility
autoclavable compatible
form
liquid
shelf life
365 days
feature
closure type White screw cap with septum and protector, ready-to-use
composition
Agar, 0.2 g , Casein Peptone, 15 g , L-Cystine, 0.5 g , Glucose Anhydrous, 5 g , NaCl, 2.5 g , Resazurin, 1 mg , Sodium Thioglycollate, 0.5 g , Yeast Extract, 5 g
packaging
pack of 6 bottles
bottle capacity
1000 mL
bottle filling volume
900 mL
pH range
6.9-7.3
application(s)
food and beverages
pharmaceutical
sterility testing
storage temp.
2-25°C
suitability
nonselective for
Quality Level
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General description
Fluid Thioglycollate Medium (FTM) Clear is a complex medium suitable for the cultivation and isolation of fastidious aerobic and anaerobic microorganisms during sterility testing of pharmaceutical products. The reduced agar content supplemented by a clear gelling agent offers extra clarity with the same media properties as FTM.
Application
Fluid Thioglycollate Medium (FTM) Clear is used as a sterility testing medium for sterile pharmaceutical products. FTM clear is used to cultivate and isolate anaerobic and microaerophilic microbes.
Biochem/physiol Actions
Thioglycollate and L-Cystine reduce the redox potential of the culture medium to create an anaerobic atmosphere. Additionally, these agents inactivate mercury and other heavy metal compounds. Agar and clear gelling agents further reduce the rapid diffusion of oxygen through the medium while offering a clear medium. Resazurin indicates the reduction potential. A color change from yellow to pink in the medium shows an increase in oxygen concentration.
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 pharmacopeia 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, thus improving accuracy and reducing the risk of incorrect interpretation and false results.
Analysis Note
The appearance of the medium is clear or almost clear and yellowish.
Other Notes
Production will take place at Millipore SAS in Molsheim, France. Deliveries will be executed in accordance with the terms and conditions of MLS RTU GmbH. A minimum order quantity is required to process the order. Once the order is placed and confirmed, Merck will ensure product delivery within a maximum timeframe of 10 to 12 weeks. The terms and conditions of Merck KGaA apply to both Millipore SAS and MLS RTU GmbH and can be accessed through the following link: Standard Terms & Conditions
This medium can be modified and/or supplemented based on the required performance criteria.
Disclaimer
This item is created at the customer′s request as a customized product and will not be developed or qualified in accordance with the Merck Product Development Process.
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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