1. Harvest cells from a culture that is at or near peak density by centrifugation at 600 x g for 5 min. Pool the cell pellets into a single tube.
2. Adjust the concentration of cells to 2.0 x 10⁶/mL.xa0 If the concentration is too low, centrifuge at 600 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
3. Prepare a 15% (v/v) sterile DMSO solution in ATCC medium 1034 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 ATCC medium 1034.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. Mix the cell preparation and the DMSO in equal portions. Thus, the final concentration will be 10⁶ and 7.5% (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. 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.
7. The frozen preparations are stored in either the vapor or liquid phase of a nitrogen refrigerator.
8. To establish a culture from the frozen state place an ampule in a water bath set at 35°C. Immerse the vial just sufficiently to cover only the frozen material. Do not agitate the vial.
9. Immediately after thawing, do not leave in the water bath, aseptically remove the contents of the ampule and inoculate into a fresh tube or flask of ATCC medium 1034.
10. Incubate at 35°C with the cap screwed on tightly (incubate a test tube on a 15° horizontal slant).

Holbrook TW, et al. Activation of the alternative complement pathway by Naegleria fowleri. Infect. Immun. 30: 58-61, 1980. PubMed: 7439979

Daggett PM, Nerad TA. The biochemical identification of vahlkampfiid amoebae. J. Protozool. 30: 126-128, 1983. PubMed: 6864593

Darby CP, et al. Primary amebic meningoencephalitis. Am. J. Dis. Child. 133: 1025-1027, 1979. PubMed: 495593

Holbrook TW, Parker BW. Naegleria fowleri in chick embryos effects of embryo age and incubation temperature, and the infectivity of embryo-derived amebae for mice. Am. J. Trop. Med. Hyg. 28: 984-987, 1979. PubMed: 574367

Holbrook TW. Naegleria fowleri in the chick embryo. Trans. R. Soc. Trop. Med. Hyg. 73: 460-462, 1979. PubMed: 555075

Olomu N, et al. Demonstration of various acid hydrolases and preliminary characterization of acid phosphatase in Naegleria fowleri. J. Protozool. 33: 317-321, 1986. PubMed: 3018238