Trypanosoma brucei Plimmer and Bradford-质粒载体-ATCC-DSM-CCUG-泰斯拓生物

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Trypanosoma brucei Plimmer and Bradford
Trypanosoma brucei Plimmer and Bradford
规格:
货期:
编号:TS149592
品牌:Testobio
产品名称: Trypanosoma brucei Plimmer and Bradford
商品货号: TS149592
Strain Designations: Lister 427 procyclic form
Biosafety Level: 2

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: Unknown; possibly derived from s427 strain, Uganda, 1960
Product Format: frozen
Storage Conditions: Frozen: -70°C or colder
Live Culture: See Protocols Section
Comments: Wild type procyclic form
Medium: ATCC® Medium 2831: SDM-79 Medium
ATCC® Medium 431: Trypanosome medium
Growth Conditions: Temperature: 27°C
Cryopreservation: Harvest and Preservation
  1. Harvest cells from a culture which is at or near peak density by centrifugation at ~800 x g for 5 min.
  2. Adjust concentration of cells to 0.5–1.0 x 107/mL in fresh growth medium. xa0If the concentration is too low, centrifuge at ~800 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
  3. While cells are centrifuging, prepare a 20% (v/v) solution of sterile glycerol in fresh growth medium.xa0
  4. Mix the cell preparation and the glycerol solution in equal portions. The final concentration will be 2.5-5 x 106 cells/mL in 10% glycerol. The time from the mixing of the cell preparation and glycerol stock solution before the freezing process is begun should be no less than 15 min and no more than 30 min.
  5. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryovials.
  6. Place the ampules 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 If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion.xa0 At -40°C, plunge ampules into liquid nitrogen.
  7. Store in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To thaw a frozen ampule, place it in a 35°C water bath such that the lip of the ampule remains above the water line. Thawing time is approximately 2 to 3 minutes.xa0 Do not agitate the ampule.xa0 Do not leave ampule in water bath after it is thawed.
  9. Remove the vial from the water bath immediately after thawing.xa0 Aseptically transfer the contents of the ampule into 10 mL of fresh growth medium.xa0
  10. Incubate the flask at 27°C with the cap screwed on tightly.
  11. Maintain as described above.xa0
Name of Depositor: G Cross
References:

Wirtz E, et al. A tightly regulated inducible expression system for conditional gene knock-outs and dominant-negative genetics in Trypanosoma brucei. Mol. Biochem. Parasitol. 99(1): 89-101, 1999. PubMed: 10215027

Cunningham MP, Vickerman K. Antigenic analysis in the Trypanosoma brucei group, using the agglutination reaction. Trans. R. Soc. Trop. Med. Hyg. 56: 48-59, 1962. PubMed: 13882652

Cross GA, Manning JC. Cultivation of Trypanosoma brucei sspp. in semi-defined and defined media. Parasitology 67(3): 315-331, 1973. PubMed: 4761771

Peacock L, et al. Fly transmission and mating of Trypanosoma brucei brucei strain 427. Mol Biochem Parasitol 160(2): 100-106, 2008. PubMed: 18524395

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Trypanosoma brucei Plimmer and Bradford

  • 货号: TS149592
  • 好评
有货
  • 品牌 : TESTOBIO
产品名称: Trypanosoma brucei Plimmer and Bradford
商品货号: TS149592
Strain Designations: Lister 427 procyclic form
Biosafety Level: 2

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: Unknown; possibly derived from s427 strain, Uganda, 1960
Product Format: frozen
Storage Conditions: Frozen: -70°C or colder
Live Culture: See Protocols Section
Comments: Wild type procyclic form
Medium: ATCC® Medium 2831: SDM-79 Medium
ATCC® Medium 431: Trypanosome medium
Growth Conditions: Temperature: 27°C
Cryopreservation: Harvest and Preservation
  1. Harvest cells from a culture which is at or near peak density by centrifugation at ~800 x g for 5 min.
  2. Adjust concentration of cells to 0.5–1.0 x 107/mL in fresh growth medium. xa0If the concentration is too low, centrifuge at ~800 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
  3. While cells are centrifuging, prepare a 20% (v/v) solution of sterile glycerol in fresh growth medium.xa0
  4. Mix the cell preparation and the glycerol solution in equal portions. The final concentration will be 2.5-5 x 106 cells/mL in 10% glycerol. The time from the mixing of the cell preparation and glycerol stock solution before the freezing process is begun should be no less than 15 min and no more than 30 min.
  5. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryovials.
  6. Place the ampules 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 If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion.xa0 At -40°C, plunge ampules into liquid nitrogen.
  7. Store in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To thaw a frozen ampule, place it in a 35°C water bath such that the lip of the ampule remains above the water line. Thawing time is approximately 2 to 3 minutes.xa0 Do not agitate the ampule.xa0 Do not leave ampule in water bath after it is thawed.
  9. Remove the vial from the water bath immediately after thawing.xa0 Aseptically transfer the contents of the ampule into 10 mL of fresh growth medium.xa0
  10. Incubate the flask at 27°C with the cap screwed on tightly.
  11. Maintain as described above.xa0
Name of Depositor: G Cross
References:

Wirtz E, et al. A tightly regulated inducible expression system for conditional gene knock-outs and dominant-negative genetics in Trypanosoma brucei. Mol. Biochem. Parasitol. 99(1): 89-101, 1999. PubMed: 10215027

Cunningham MP, Vickerman K. Antigenic analysis in the Trypanosoma brucei group, using the agglutination reaction. Trans. R. Soc. Trop. Med. Hyg. 56: 48-59, 1962. PubMed: 13882652

Cross GA, Manning JC. Cultivation of Trypanosoma brucei sspp. in semi-defined and defined media. Parasitology 67(3): 315-331, 1973. PubMed: 4761771

Peacock L, et al. Fly transmission and mating of Trypanosoma brucei brucei strain 427. Mol Biochem Parasitol 160(2): 100-106, 2008. PubMed: 18524395

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