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Medio de tioglicolato líquido

Name: Medio de tioglicolato líquido
Brand: MM

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

Sinónimos:

Fluid Thioglycollate Medium acc EP+USP, Fluid Thioglycollate Medium, FTM, Thioglycollate Broth

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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

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Propiedades

Quality Segment

300

agency

EP 2.6.1, JP 4.06, USP 71

sterility

sterile

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))

technique(s)

sterile filtration: suitable

bottle capacity

125 mL

bottle filling volume

100 mL

pH

7.1

application(s)

cosmetics
food and beverages
microbiology
pharmaceutical
sterility testing

storage temp.

2-25°C

suitability

aerobic bacteria, anaerobic bacteria

Descripción

General description

Fluid Thioglycolate Medium is a universal complex medium with thioglycollate and L-Cystine to reduce the redox potential of the culture medium and create an anaerobic atmosphere. They also inactivate mercury and other heavy metal compounds. Agar in the medium further reduces the rapid diffusion of oxygen but may lead to slight turbidity in larger volumes (filled bottles). Resazurin indicates the reduction potential of the medium. An increased concentration of oxygen is indicated by a color change to pink.

Application

Fluid Thioglycolate Medium is suitable for the isolation and cultivation of fastidious anaerobic as well as for aerobic microorganisms. It is used 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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