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Molecular biology media

YP Agar Base Medium

For maintaining and developing yeast in molecular biology procedures.

Cat. No.
LC-1513
Format
500 g
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months

YP Agar Base Medium is used for the maintenance and the development of yeast in molecular biology procedures.

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Cat. No.FormatPrice
LC-1513500 g

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Key features

Applications

Growth of yeasts.

Industry

Culture media for molecular biology.

Preparation

50 g in 900 mL of distilled water; boil for one minute, sterilize in autoclave at 121 °C for 15 minutes, add 100 mL of sterile dextrose at 20%.

Principles and uses

YP Agar Base Medium is also used to cultivate Saccharomyces cerevisiae and other yeasts. Yeasts grow well on a medium containing only a minimal amount of glucose and salts. This medium contains glucose (with the addition of dextrose after autoclaving), salts and proteins, which favours the growth of Saccharomyces cerevisiae and reduces growing times. Yeast extract is the source of vitamins, particularly the B-group, essential for bacterial growth. Peptone provides nitrogen, vitamins, minerals and amino acids. Bacteriological agar is the solidifying agent.

Saccharomyces cerevisiae has a genome of 14 Mb containing 6000 genes arranged in 16 chromosomes, which have been completely sequenced, and thus, is a species type in microbiology and genetics studies.

Technical specifications

SolubilityWithout residues
AppearanceFine powder
Color of the dehydrated mediumBeige
Color of the prepared mediumClear amber, slightly opalescent
Final pH (25 °C)7.0 ± 0.2
Amount50 g in 900 mL
Storage2 to 25 °C

Formula

Ingredientg/L
Bacteriological agar20
Peptone20
Yeast extract10

Preparation and use

Preparation

Suspend 50 grams of the dehydrated medium in 900 mL of distilled water. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. Sterilize in autoclave at 121 °C for 15 minutes. Cool to room temperature and aseptically add 100 mL of sterile dextrose at 20%. Mix well and dispense into appropriate containers.

Instructions for use

Pour plate method:

  1. Deposit 1 mL of the initial suspension and/or diluted sample in an empty Petri dish.
  2. Add 12-15 mL of agar cooled to 44-47 °C in each Petri dish and mix gently moving the plate.
  3. Allow the plates to solidify and incubate in an inverted position at a temperature of 25 ± 2 °C for 42-48 hours.

Streak plate method:

  1. In a Petri dish, add 12-15 mL of molten agar and let it solidify.
  2. Inoculate 10 µL of the initial suspension and/or diluted sample.
  3. Extend the inoculum with a sterile loop on the agar surface.
  4. Incubate the plates in an inverted position at a temperature of 25 ± 2 °C for 42-48 hours.

Quality control

Microbiological test

Incubation conditions: 25 ± 2 °C / 42-48 h.

MicroorganismSpecification
Candida albicansATCC 10231Good growth
Saccharomyces cerevisiaeATCC 9763Good growth

Bibliography

  • Guide to yeast genetics and molecular biology. (1991) Ed. Christine Guthrie & Gerald Fink. Methods in Enzymology vol. 194.
  • Current protocols in Molecular Biology. Eds. Ausubel, F. M. Brent, R., Kingston, R, E., Moore, D. D., Seidman, J. G., Smith J. A., and Struhl, K. 13,01.-13.2.10.
  • The Yeast Genome Directory (1997, May 29) Nature Supp. to volume 387.
  • The condensed protocols from molecular cloning: a laboratory manual / Joseph Sambrook, David W. Russell.

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Shipped under controlled temperature when the product requires it.

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Frequently asked questions

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