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微信小章| 产品名称： | Trypanosoma cruzi Chagas |
|---|---|
| 商品货号： | TS171789 |
| Strain Designations： | SYLVIO-X10 |
| 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： | obtained from the fifth instar of Rhodnius prolixus used for xenodiagnosis of an acute case of slyvatic-derived Chagas disease, Para, Brazil, 1978 |
| Product Format： | frozen |
| Type Strain： | no |
| Medium： | ATCC® Medium 1029: LIT medium |
| Growth Conditions： | Temperature: 25.0°C Duration: axenic |
| Cryopreservation： | 1.xa0xa0 Harvest cells from a culture that is at or near peak density by centrifugation at ~800 x g for 5 min. Pool the cell pellets into a single tube. 2.xa0xa0 Adjust the concentration of cells to 2.0 x 107/ml.xa0 If 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.xa0xa0 Prepare a 10% (v/v) sterile DMSO solution in fresh medium as follows:xa0 Add the required volume of DMSO to a glass screw-capped test tube and place on ice.xa0 Allow the DMSO to solidify.xa0 Add the required volume of refrigerated medium.xa0 Dissolve the DMSO by inverting several times.xa0 If the DMSO solution is not prepared on ice, an exothermic reaction will occur that may precipitate certain components of the medium. 4.xa0xa0 Mix the cell preparation and the DMSO in equal portions. Thus, the final concentration will be 107 and 5% (v/v) DMSO. The time from the mixing of the cell preparation and DMSO stock solution to the start of the freezing process should be no less than 15 min and no longer than 60 min. 5.xa0xa0 Dispense in 0.5 ml aliquots into 1.0 - 2.0 ml sterile plastic screw-capped cryules (special plastic vials for cryopreservation). 6.xa0 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. 7.xa0xa0 The frozen preparations are stored in either the vapor or liquid phase of a nitrogen refrigerator. 8.xa0xa0 To establish a culture from the frozen state place an ampule in a water bath set at 35°C. Immerse the vial enough to cover only the frozen material. Do not agitate the vial. 9.xa0xa0 Immediately after thawing, do not leave in the water bath, aseptically remove the contents of the ampule and inoculate into 10.0 ml of fresh ATCC medium 1029. 10.xa0xa0xa0xa0xa0xa0xa0xa0xa0 Incubate the tube at 20-25°C with the cap screwed on tightly. |
| Name of Depositor： | JA Dvorak |
| Special Collection： | NCRR Contract |
| Year of Origin： | 1978 |
| References： | Dvorak JA, et al. Trypanosoma cruzi: flow cytometric analysis. I. Analysis of total DNA/organism by means of mithramycin-induced fluorescence. J. Protozool. 29: 430-437, 1982. PubMed: 6182288 Postan M, et al. Studies of Trypanosoma cruzi clones in inbred mice. I. A comparison of the course of infection of C3H/HEN- mice with two clones isolated from a common source. Am. J. Trop. Med. Hyg. 32: 497-506, 1983. PubMed: 6407346 |