| 产品名称： |
Ulothrix gigas (Vischer) Mattox and Bold |
| 商品货号： |
TS206536 |
| Deposited As： |
Uronema gigas Vischer |
| Strain Designations： |
UTEX 174 CCAP-386/3 |
| Application： |
algal resistance testing paint |
| Biosafety Level： |
1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Isolation： |
Freshwater, Switzerland, 1930 |
| Product Format： |
frozen |
| Storage Conditions： |
Frozen Cultures:
-70°C for 1 week; liquid N2 vapor for long term storage
Freeze-dried Cultures:
2-8°C
Live Cultures:
See Protocols section for handling information |
| Type Strain： |
no |
| Comments： |
This strain is recommended by ATCC for use in the tests described in ASTM Standard Test Method E1366-91 where only the taxon is specified. photosynthetic |
| Medium： |
ATCC® Medium 847: Algal proteose agar
|
| Growth Conditions： |
Temperature: 25°C
Culture System: Axenic |
| Cryopreservation： |
Harvest and Preservation
- Harvest cells from a culture that is at or near peak density by centrifugation at 800 x g for 5 min.
- Adjust the concentration of cells to 2 x 106 - 2 x 107/mL in fresh broth medium.
- While cells are centrifuging prepare a 14% (v/v) solution of sterile DMSO in fresh broth medium.
- Mix the cell preparation and the 14% DMSO in equal portions. Thus, the final concentration will be 106 - 107 cells/mL and 7% (v/v) DMSO. The time from the mixing of the cell preparation and DMSO stock solution to the beginning of the freezing process should be no less than 5 min and no greater than 15 min.
- Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
- Place the vials in a controlled rate freezing unit.xa0 From room temperature cool at -1°C/min to -40°C.xa0 If the freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through the heat of fusion.xa0 At -40°C plunge into liquid nitrogen. Alternatively, place the vials in a Nalgene 1°C freezing apparatus.xa0 Place the apparatus at -80°C for 1.5 to 2 hours and then plunge ampules into liquid nitrogen.xa0 (The cooling rate in this apparatus is approximately -1°C/min.) xa0
- The frozen preparations should be stored in either the vapor or liquid phase of a nitrogen refrigerator. Frozen preparations stored below -130°C are stabile indefinitely. Those stored at temperatures above -130°C are progressively less stabile as the storage temperature is elevated. Vials should not be stored above -55°C.
- To establish a culture from the frozen state place an ampule in a water bath set at 35°C. Immerse the vial just to a level just above the surface of the frozen material. Do not agitate the vial.
- Immediately after thawing, do not leave in the water bath, aseptically remove the contents of the ampule and inoculate a 16 x 125 mm screw-capped test tube containing 5 mL of ATCC medium 847 broth.
- Incubate the culture on a 15° horizontal slant at 25°C with the cap screwed on loosely (loosened one-half turn) and incubate under a 14 hour light (~50 µEinsteins/m2/s irradiance)/10 hour dark cycle.
|
| Name of Depositor： |
UTEX |
| Chain of Custody： |
ATCC <-- UTEX <-- . . . <-- W. Vischer strain 69 |
| Year of Origin： |
1930 |
| References： |
Starr RC. The culture collection of algae at Indiana University. Am. J. Bot. 51: 1013-1044, 1964.
Standard Test Method for Determining the Resistance of Paint Films and Related Coatings to Algal Defacement. West Conshohocken, PA:ASTM International;ASTM Standard Test Method D 5589-97 (Reapproved 2002).
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