Euglena Medium

UTEX sells Euglena Medium at 1X concentration only. Stock solutions and individual components for this specific medium are currently not available for purchase.

Euglena Medium

Freshwater Medium | 6 < pH < 8

Organic N Organic Supplements

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$ 55.00

Euglena Medium

Suitable for most axenic cultures of Euglena and Chlorogonium.

Directions

For 1 L Total

To approximately 950 mL of dH₂O, add each of the components in the order specified while stirring continuously.
Bring the total volume to 1 L with dH₂O.
- For 1.5% agar medium add 15 g of agar into the flask; do not mix.
Cover and autoclave medium.
Store at refrigerator temperature.

#
1
Component	Sodium acetate (Fisher BP 333)
Amount	1 g/L
Final Concentration	12.2 mM
2
Component	Beef extract (Sigma B-4888)
Amount	1 g/L
3
Component	Tryptone (Sigma T 9410))
Amount	2 g/L
4
Component	Yeast extract (Bacto, Difco)
Amount	2 g/L
5
Component	CaCl₂•2H₂O (Sigma C-3881)
Amount	0.01 g/L
Final Concentration	0.07 mM

#	Component	Amount	Final Concentration
1	Sodium acetate (Fisher BP 333)	1 g/L	12.2 mM
2	Beef extract (Sigma B-4888)	1 g/L
3	Tryptone (Sigma T 9410))	2 g/L
4	Yeast extract (Bacto, Difco)	2 g/L
5	CaCl₂•2H₂O (Sigma C-3881)	0.01 g/L	0.07 mM

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Euglena Medium Recipe PDF

Safety Data Sheet (SDS)

FAQs:Algal Culture Media

Important Notes To Consider:

The quality of water, including natural seawater, is important. The term 'dH₂O' generally refers to distilled, deionized, distilled/deionized water, Milli-Q water (Millipore Corp.), etc. Natural seawater and natural freshwater should be obtained from a non-polluted source.
When dissolving chemicals, wait for the first component to dissolve before adding the second. Stirring, and sometimes the addition of heat, is often required to dissolve the chemicals efficiently. Preparation of stock solutions for frequently made algal culture media make preparing media convenient but also necessary to avoid errors from weighing very tiny amounts.
Attention should be given to the pH of the final medium. In most cases, if pH adjustment is required, this occurs before sterilization. Please note that autoclaving removes carbon dioxide from media lacking carbonate stabilizing buffers. This would make the medium very alkaline soon after removal from the autoclave. In these cases, you should wait approximately 24 hours for gaseous equilibrium before inoculating the medium.