| 產(chǎn)品名稱 |
Lotmaria passim |
| 商品貨號(hào) |
B219448 |
| Deposited As |
Crithidia mellificae |
| Strain Designations |
SF |
| Biosafety Level |
1
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 |
Honey bee gut, 2010, CA |
| Product Format |
frozen |
| Storage Conditions |
Frozen Cultures:
-70°C for 1 week; liquid N2 vapor for long term storage
Freeze-dried Cultures:
2-8°C
Live Cultures:
See Protocols section for handling information |
| Genome Sequenced Strain |
Yes
|
| Comments |
This item is presently archived as original material and is available on a "made-to-order" basis.
Genome strain |
| Medium |
ATCC® Medium 1034: Modified PYNFH medium (Available from ATCC as ATCC cat. no. 327-X)
|
| Growth Conditions |
Temperature: 20°C to 25°C
Atmosphere: Aerobic
|
| Cryopreservation |
Reagents
Cryoprotective Solution
DMSO, 1.0 mL
Fresh complete growth medium, 9.0 mL
Harvest and Preservation
- Harvest cells from a culture which is at or near peak density by centrifugation at 800-1000 x g for 5 min.
- Adjust concentration of cells to between 2 x 107 and 2 x 108 cells/mL in fresh medium. If the cell concentration is too low, centrifuge at 800-1000 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
- While cells are centrifuging, prepare a 10% (v/v) solution of sterile DMSO in fresh medium (broth). The DMSO solution when first prepared will warm up due to chemical heat. The solution should be allowed to return to room temperature prior to use.
- Mix the cell preparation and the DMSO solution in equal portions. The final concentration will be 107 – 108 cells/mL 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 more than 30 min.
- Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
- Place the ampules in a Nalgene 1°C freezing apparatus. Place the apparatus at -80°C for 1.5 to 2 hours and then plunge ampules into liquid nitrogen. (The cooling rate in this apparatus is approximately -1°C/min.) 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.
- Store in either the vapor or liquid phase of a nitrogen refrigerator.
- To establish a culture from the frozen state, place an ampule in a 35°C water bath (2-3 min). Immerse the vial just sufficiently to cover the frozen material. Do not agitate the vial.
- Remove the vial from the water bath immediately after thawing. Aseptically transfer the entire contents of the ampule into a T-25 tissue culture flask containing 10.0 mL complete medium. Incubate with the cap tightly sealed at 20-25°C.
- Maintain as described above.
|
| Name of Depositor |
J DeRisi |
| Chain of Custody |
ATCC <-- J DeRisi |
| References |
Runckel C, et al. Temporal analysis of the honey bee microbiome reveals four novel viruses and seasonal prevalence of known viruses, Nosema, and Crithidia. PLoS One 6(6): e20656, 2011. PubMed: 21687739
|
