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Acanthamoeba sp. 菌株拉丁名

(ATCC® PRA-2™) 菌株編號(hào)

Strain Designations 菌株別名 : UWC8 /

Depositor: TR Fritsche /

Biosafety Level 生物安全等級(jí) : 2

Strain Designations 菌株別名 UWC8

Biosafety Level 生物安全等級(jí) 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 分離源 clinical specimen - human

Product Format 提供形式 frozen

Type Strain 模式菌株 no

Medium 培養(yǎng)基 ATCC® Medium 712: PYG w/ Additives

Growth Conditions 生長(zhǎng)條件

Temperature 培養(yǎng)溫度 : 25.0℃

Duration: monoxenic

Cryopreservation 1. To achieve the best results set up cultures with several different inocula (e.g. 0.25 ml, 0.5 ml, 1.0 ml). Harvest cultures and pool when the culture that received the lowest inoculum is at or near peak density.

2. If the cell concentration exceeds the required level do not centrifuge, but adjust the concentration to between 2 x 106 and 2 x 107cysts/ml with fresh medium.

If the concentration is too low, centrifuge at 600 x g for 5 min and resuspend the pellet in the volume of fresh medium required to yield the desired concentration.

3. While cells are centrifuging prepare a 15% (v/v) solution of sterile DMSO as follows: Add the required volume of DMSO to a glass screw-capped test tube and place it in an ice bath. Allow the DMSO to solidify.

Add the required volume of refrigerated medium. Dissolve the DMSO by inverting the tube several times.

*NOTE: 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 between 106 and 107 cells/ml and 7.5% (v/v) DMSO.

The time from the mixing of the cell preparation and DMSO stock solution before the freezing process is begun should be no less than 15 min and no longer than 30 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 the vials in a controlled rate freezing unit. From room temperature cool at -1℃/min to -40℃.

If the freezing unit can compensate for the heat of fusion, maintain rate at -1℃/min through the heat of fusion. At -40℃ plunge into liquid nitrogen.

Alternatively, place the vials in a Nalgene 1℃ freezing apparatus. Place the apparatus at -80℃ for 1.5 to 2 hours and then plunge ampules into liquid nitrogen.

(The cooling rate in this apparatus is approximately -1℃/min.)

7. The frozen preparations are stored in either the vapor or liquid phase of a nitrogen freezer.

8. To establish a culture from the frozen state place an ampule in a water bath set at 35℃ (2-3 min). Immerse the vial just sufficient to cover the frozen material. Do not agitate the vial.

9. Immediately after thawing, aseptically remove the contents of the ampule and inoculate into 5 ml of fresh ATCC medium 712 in a T-25 tissue culture flask or plastic 16 x 125 mm screw-capped test tube. Incubate at 25℃.

Name of Depositor 寄存人 TR Fritsche

Special Collection NCRR Contract

References 參考文獻(xiàn) Gautom RK, Fritsche TR. Transmissibility of bacterial endosymbionts between isolates of Acanthamoeba spp.. J. Eukaryot. Microbiol. 42: 452-456, 1995. PubMed: 7581321

Fritsche TR, et al. In situ detection of novel bacterial endosymbionts of Acanthamoeba spp. phylogenetically related to members of the order Rickettsiales. Appl. Environ. Microbiol. 65: 206-212, 1999. PubMed: 9872781

corneal scrapings from human keratitis patient, Seattle, WA contains a bacterial endosymbiont

Cross References Nucleotide (GenBank) : AF069963 16S ribosomal RNA gene, partial sequence from endosymbiont