Diplophrys parva-质粒载体-ATCC-DSM-CCUG-泰斯拓生物

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Diplophrys parva
Diplophrys parva
规格:
货期:
编号:TS147134
品牌:Testobio
产品名称： Diplophrys parva Anderson and Cavalier-Smith
商品货号： TS147134
Deposited As： Diplophrys sp.
Strain Designations： GF
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： Intestinal tract, goldfish, Carassius auratus, Baltimore, MD, 1992
Product Format： frozen
Storage Conditions： Frozen: -70°C or colder
Freeze-Dried: 2°C to 8°C
Live Culture: See Protocols Section
Type Strain： yes
Medium： ATCC® Medium 802: Sonneborns Paramecium medium
Growth Conditions：
Temperature: 25°C
Culture System: Xenic, grown with Enterobacter aerogenes (ATCC® 13048™) and mixed bacteria
Cryopreservation： Reagents
Cryoprotective Solution
DMSO, 1.5 mL
Fresh growth medium w/o bacteria, 8.5 mL


Harvest and Preservation
  1. Mix the components in the order listed. When the medium is added to the DMSO the solution will warm up due to chemical heat.
  2. Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 800 x g for 5 min.
  3. Adjust the concentration of cells to at least 2 x 106/mL in fresh medium.
  4. Mix the cell preparation and the cryoprotective solution in equal portions.
  5. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
  6. 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.) xa0
  7. Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator.
  8. 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.xa0xa0 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 media 802 and 2348, combined in equal parts and bacterized with Klebsiella pneumoniae subsp. pneumoniae (ATCC® 700831™) or Enterobacter aerogenes (ATCC® 13048™).
  9. Incubate at 25°C with the cap screwed on tightly.
  10. Once the culture is established, vigorously agitate the flask and aseptically transfer 0.5 mL to 10.0 mL of bacterized medium.
  11. Follow the protocol for maintenance of culture.
Name of Depositor： SA Schaffer
Year of Origin： 1992
References：

Anderson OR, et al. Ultrastructure of Diplophrys parva, a new small freshwater species, and a revised analysis of Labyrinthulea (Heterokonta). Acta Protozool. 51: 291-304, 2012.

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Diplophrys parva

  • 货号: TS147134
  • 好评
有货
  • 品牌 : TESTOBIO
产品名称： Diplophrys parva Anderson and Cavalier-Smith
商品货号： TS147134
Deposited As： Diplophrys sp.
Strain Designations： GF
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： Intestinal tract, goldfish, Carassius auratus, Baltimore, MD, 1992
Product Format： frozen
Storage Conditions： Frozen: -70°C or colder
Freeze-Dried: 2°C to 8°C
Live Culture: See Protocols Section
Type Strain： yes
Medium： ATCC® Medium 802: Sonneborns Paramecium medium
Growth Conditions：
Temperature: 25°C
Culture System: Xenic, grown with Enterobacter aerogenes (ATCC® 13048™) and mixed bacteria
Cryopreservation： Reagents
Cryoprotective Solution
DMSO, 1.5 mL
Fresh growth medium w/o bacteria, 8.5 mL


Harvest and Preservation
  1. Mix the components in the order listed. When the medium is added to the DMSO the solution will warm up due to chemical heat.
  2. Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 800 x g for 5 min.
  3. Adjust the concentration of cells to at least 2 x 106/mL in fresh medium.
  4. Mix the cell preparation and the cryoprotective solution in equal portions.
  5. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
  6. 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.) xa0
  7. Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator.
  8. 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.xa0xa0 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 media 802 and 2348, combined in equal parts and bacterized with Klebsiella pneumoniae subsp. pneumoniae (ATCC® 700831™) or Enterobacter aerogenes (ATCC® 13048™).
  9. Incubate at 25°C with the cap screwed on tightly.
  10. Once the culture is established, vigorously agitate the flask and aseptically transfer 0.5 mL to 10.0 mL of bacterized medium.
  11. Follow the protocol for maintenance of culture.
Name of Depositor： SA Schaffer
Year of Origin： 1992
References：

Anderson OR, et al. Ultrastructure of Diplophrys parva, a new small freshwater species, and a revised analysis of Labyrinthulea (Heterokonta). Acta Protozool. 51: 291-304, 2012.

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