HM Peptone B Agar (Meat extract B Agar)

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SKU:
M806
Used for routine cultivation of non fastidious bacteria.


Intended use

Used for routine cultivation of non fastidious bacteria.

Composition**

Ingredients g/L
Peptone 10.000
HM peptone B# 3.000
Sodium chloride 5.000
Agar 15.000
Final pH (at 25°C) 7.6±0.2

**Formula adjusted, standardized to suit performance parameters

# Equivalent to Beef extract

Directions

Suspend 33.0 grams in 1000 ml purified / distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool to 45-50°C. Mix well and pour the medium in sterile Petri plates.

Principle And Interpretation

The majority of organisms to be studied in medical bacteriology are either pathogens or commensals of the human body, and in order to obtain suitable growth the artificial culture medium should provide nutrients and a pH (about 7.2) approximating to those of the tissues and body fluids. For routine purposes many of these nutrients are supplied by aqueous extracts of peptone, which is a product of the digestion of protein (1).

HM Peptone B Agar can be used as a general-purpose nutrient medium and is also recommended for preparation of pure culture of Candida species for carrying out fermentation studies (2). HM Peptone B Agar is a non-selective nutrient medium containing HM peptone B and peptone as a source of nitrogen and carbon and sodium chloride as a source of electrolytes.

Type of specimen

Clinical samples - urine, faeces, pus, etc.; Food and dairy sample; Water samples

Specimen Collection and Handling:

For clinical samples follow appropriate techniques for handling specimens as per established guidelines (3,4). For food and dairy samples, follow appropriate techniques for sample collection and processing as per guidelines (5,6,7). For water samples, follow appropriate techniques for sample collection, processing as per guidelines and local standards. (8) After use, contaminated materials must be sterilized by autoclaving before discarding.

Warning and Precautions :

In Vitro diagnostic Use. For professional use only. Read the label before opening the container. Wear protective gloves/ protective clothing/eye protection/ face protection. Follow good microbiological lab practices while handling specimens and culture. Standard precautions as per established guidelines should be followed while handling clinical specimens. Safety guidelines may be referred in individual safety data sheets.

Limitations :

  • This medium is general purpose medium and may not support the growth of fastidious organisms.
  • Further biochemical and serological tests must be performed for confirmation.

Performance and Evaluation

Performance of the medium is expected when used as per the direction on the label within the expiry period when stored at recommended temperature.

Quality Control

Appearance
Cream to yellow homogeneous free flowing powder.

Gelling
Firm, comparable with 1.5% Agar gel

Colour and Clarity of prepared medium
Yellow coloured, clear to slightly opalescent gel forms in Petri plates

Reaction
Reaction of 3.3% w/v aqueous solution at 25°C. pH: 7.6±0.2

pH
7.40-7.80

Cultural Response
Cultural characteristics observed after an incubation at 35-37°C for 18-48 hours.

Organism Inoculum (CFU) Growth Recovery
Candida albicans ATCC 10231 (00054*) 50-100 luxuriant >=70%
Escherichia coli ATCC 25922 (00013*) 50-100 luxuriant >=70%
Pseudomonas aeruginosa ATCC 27853 (00025*) 50-100 luxuriant >=70%
Salmonella Typhi ATCC 6539 50-100 luxuriant >=70%
Staphylococcus aureus subsp. aureus ATCC 25923 (00034*) 50-100 luxuriant >=70%

Key: *Corresponding WDCM numbers.

Storage and Shelf Life

Store below 10-30°C in a tightly closed container and the prepared medium at 20-30°C. Use before expiry date on the label. On opening, product should be properly stored dry, after tightly capping the bottle inorder to prevent lump formation due to the hygroscopic nature of the product. Improper storage of the product may lead to lump formation. Store in dry ventilated area protected from extremes of temperature and sources of ignition Seal the container tightly after use. Product performance is best if used within stated expiry period.

Disposal

User must ensure safe disposal by autoclaving and/or incineration of used or unusable preparations of this product. Follow established laboratory procedures in disposing of infectious materials and material that comes into contact with clinical sample must be decontaminated and disposed of in accordance with current laboratory techniques (3,4).

More Information
Product Name HM Peptone B Agar (Meat extract B Agar)
SKU M806
Product Type Regular
Physical Form Powder
Origin Animal
Packaging type HDPE
References 1. Collee J. G., Fraser A. G., Marimon B. P., Simmons A., (Eds.) ,1996, Mackie and McCartney Practical Medical Microbiology,14th Ed., Churchill Livingstone.2.Finegold S. M. and Baron E. J., (Ed.), Bailey and Scott's Diagnostic Microbiology, 1986, 7th Edition, The C.V. MosbyCompany, St. Louis.3.Isenberg, H.D. Clinical Microbiology Procedures Handb0ook. 2nd Edition.4.Jorgensen,J.H., Pfaller , M.A., Carroll, K.C., Funke, G., Landry, M.L., Richter, S.S and Warnock., D.W. (2015)Manual of Clinical Microbiology, 11th Edition. Vol. 1.5.American Public Health Association, Standard Methods for the Examination of Dairy Products, 1978, 14th Ed., WashingtonD.C.6.Salfinger Y., and Tortorello M.L. Fifth (Ed.), 2015, Compendium of Methods for the Microbiological Examination ofFoods, 5th Ed., American Public Health Association, Washington, D.C.7.Wehr H. M. and Frank J. H., 2004, Standard Methods for the Microbiological Examination of Dairy Products, 17th Ed.,APHA Inc., Washington, D.C.8.Baird R.B., Eaton A.D., and Rice E.W., (Eds.), 2015, Standard Methods for the Examination of Water and Wastewater,23rd ed., APHA, Washington, D.C.9.Lapage S., Shelton J. and Mitchell T., 1970, Methods in Microbiology', Norris J. and Ribbons D., (Eds.), Vol. 3A, AcademicPress, London.10.MacFaddin J. F., 2000, Biochemical Tests for Identification of Medical Bacteria, 3rd Ed., Lippincott, Williams and Wilkins,Baltimore.
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