宁波泰斯拓生物

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浙江省宁波市镇海区庄市街道兴庄路9号创e慧谷42号楼B幢401室
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Trypanosoma cruzi Chagas

货号 TS132129
中文名称 null
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产品名称: Trypanosoma cruzi Chagas
商品货号: TS132129
Strain Designations: Tulahuen
Application:
Vector borne research
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:
Triatoma infestans, Tulahuen, Chile, 1945
Product Format: frozen
Storage Conditions: Frozen: -70°C or colder for 1 week, vapor phase of liquid nitrogen for long-term storage
Type Strain: no
Comments:
Glucose catabolist
Proteinases
Cryopreservation:

Tyrodes Salt Solution
NaCl, 8.00 g
KCl, 0.20 g
CaCl2,xa00.20 g
MgCl2 · H2O, 0.05 g
NaH2PO4 · H2O, 1.00 g
NaHCO3 · H2O, 1.00 g
Glucose, 1.00 g
Glass distilled H2O to 1.00 L
Add ingredients in the sequence listed.xa0 Filter-sterilize.

Harvest and Preservation

  1. Harvest the parasites according to the protocol for maintenance in vivo.
  2. Spin the cell suspension at approximately 50 x g for 3 min, to remove any cellular debris.
  3. Transfer the supernatant to a new 15 ml plastic centrifuge tube.xa0 Centrifuge at 1300 x g for 10 min.
  4. Pool the cell pellets and adjust the concentration to 2.0 - 4.0 x 107 cells/ml with a fresh solution of Tyrodes Salt Solution.
    *If the concentration is too low centrifuge at 1300 x g for 10 min and resuspend in the volume of Tyrodes Salt Solution required to yield the desired concentration.
  5. Mix the cell preparation and 10% (v/v) DMSO in equal portions.xa0 The final concentration will be 1.0 - 2.0 x 107 cells/ml and 5% DMSO.xa0 The time from the mixing of the cell preparation and cryoprotective solution to the start of the freezing process should be no less than 15 min. and no more than 30 min.
  6. Dispense in 0.5 ml aliquots to 1.0-2.0 ml sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
  7. 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 atxa0xa0xa0xa0xa0xa0xa0 -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.)xa0xa0
  8. Store in either the vapor or liquid phase of a nitrogen refrigerator.
  9. 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 thawed.
  10. Immediately after thawing, aseptically remove the contents of the ampule with a syringe and inoculate an uninfected mouse.xa0 Follow the protocol for maintenance in vivo.
Name of Depositor: RG Yaeger
Chain of Custody:
ATCC <-- RG Yaeger <-- T. Pizzi
Year of Origin: 1945
References:

. . Exp. Parasitol. 9: 215-222, 1960.

Redman CA, Coombs GH. The products and pathways of glucose catabolism in Herpetomonas muscarum ingenoplastis and Herpetomonas muscarum muscarum. J. Eukaryot. Microbiol. 44: 46-51, 1997.

Coombs GH. Proteinases of Leishmania mexicana and other flagellate protozoa. Parasitology 84: 149-155, 1982. PubMed: 6460959