Microstomoeca roanoka

Microstomoeca roanoka

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货期:

编号:TS135236

品牌:Testobio

产品名称：	Microstomoeca roanoka Carr, Richter and Nitsche
商品货号：	TS135236
Deposited As：	Salpingoeca sp.
Strain Designations：	BSE-01190019
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：	Dry salt marsh sediment, Hog Island, eastern shore of Virginia, 2000
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
Medium：	ATCC^® Medium 1525: Seawater 802 medium
Growth Conditions：	Temperature: 25°C Culture System: Xenic
Cryopreservation：	Reagents Cryoprotective Solution DMSO, 2.0 mL Fresh growth medium w/o bacteria, 8.0 mL Harvest and Preservation Mix the components in the order listed. When the medium is added to the DMSO the solution will warm up due to chemical heat. Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 800 x g for 5 min. Adjust the concentration of cells at least 2 x 10⁶/mL in fresh medium. Mix the cell preparation and the cryoprotective solution in equal portions. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation). Place vials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1 C/min through heat of fusion. At -40°C plunge ampules 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.)xa0xa0 Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator. To establish a culture from the frozen state place the vial in a 35°C water bath.xa0 Immerse the vial to a level just above the surface of the frozen material. Do not agitate the vial.xa0 Immediately after thawing, do not leave in water bath, aseptically remove the contents of the ampule and inoculate into a T-25 tissue culture flask containing 10 mL ATCC medium 1525 bacterized with Klebsiella pneumoniae subsp. pneumoniae (ATCC^®xa0700831™). Incubate at 25°C with the cap screwed on tightly. Once the culture is established, vigorously agitate the flask and aseptically transfer 0.5 mL to 10.0 mL of bacterized ATCC medium 1525. Follow the protocol for maintenance of culture.
Name of Depositor：	TA Nerad
Year of Origin：	2000
References：	Thomas A Nerad, personal communication

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Microstomoeca roanoka

货号: TS135236
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产品名称：	Microstomoeca roanoka Carr, Richter and Nitsche
商品货号：	TS135236
Deposited As：	Salpingoeca sp.
Strain Designations：	BSE-01190019
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：	Dry salt marsh sediment, Hog Island, eastern shore of Virginia, 2000
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
Medium：	ATCC^® Medium 1525: Seawater 802 medium
Growth Conditions：	Temperature: 25°C Culture System: Xenic
Cryopreservation：	Reagents Cryoprotective Solution DMSO, 2.0 mL Fresh growth medium w/o bacteria, 8.0 mL Harvest and Preservation Mix the components in the order listed. When the medium is added to the DMSO the solution will warm up due to chemical heat. Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 800 x g for 5 min. Adjust the concentration of cells at least 2 x 10⁶/mL in fresh medium. Mix the cell preparation and the cryoprotective solution in equal portions. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation). Place vials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1 C/min through heat of fusion. At -40°C plunge ampules 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.)xa0xa0 Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator. To establish a culture from the frozen state place the vial in a 35°C water bath.xa0 Immerse the vial to a level just above the surface of the frozen material. Do not agitate the vial.xa0 Immediately after thawing, do not leave in water bath, aseptically remove the contents of the ampule and inoculate into a T-25 tissue culture flask containing 10 mL ATCC medium 1525 bacterized with Klebsiella pneumoniae subsp. pneumoniae (ATCC^®xa0700831™). Incubate at 25°C with the cap screwed on tightly. Once the culture is established, vigorously agitate the flask and aseptically transfer 0.5 mL to 10.0 mL of bacterized ATCC medium 1525. Follow the protocol for maintenance of culture.
Name of Depositor：	TA Nerad
Year of Origin：	2000
References：	Thomas A Nerad, personal communication

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