| 产品名称： |
Diaphanoeca grandis Ellis |
| 商品货号： |
TS192964 |
| Strain Designations： |
1/19/82 NB (3) |
| Application： |
Phylogenetic analysis of SSU rRNA, LSU rRNA, tubA, and hsp-90 |
| 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： |
Narragansett Bay, RI, 1982 |
| Product Format： |
test tube |
| Storage Conditions： |
Test Tube: See handling procedure |
| Type Strain： |
no |
| Comments： |
phylogeny Phylogenetic analysis of SSU rRNA, LSU rRNA, tubA, and hsp-90 |
| Medium： |
ATCC® Medium 1405: HESNW medium
ATCC® Medium 1361: Marine flagellate medium
|
| Growth Conditions： |
Temperature:xa04-18°C (best growth is achieved at 8-10°C) |
| Cryopreservation： |
Cryoprotective Solution
DMSO, 2.0 ml
Fresh growth medium w/o bacteria, 8.0 ml
- Mix the components in the order listed. When the medium is added to the DMSO the solution will warm up due to chemical heat.xa0 Cool on ice prior to use.
- Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 800 x g for 5 min.
- Adjust the concentration of cells at least 2 x 106/ml in fresh, ice-cold medium.
- Mix the cell preparation and the cryoprotective solution in equal portions.
- Dispense in 0.5 ml aliquots into 1.0 - 2.0 ml sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
- 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. 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.) xa0
- Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator.
- To establish a culture from the frozen state place the vial in a 35°C water bath.xa0 Immerse the vial to a level just above the surface of the frozen material. xa0Do not agitate the vial.xa0 Do not allow ampule to overheat.xa0 Immediately after thawing, do not leave in water bath, aseptically remove the contents of the ampule and inoculate into a T-25 tissue culture flask containing 10 ml of ice-cold ATCC medium 1405 and two sterile rice grains.
- Incubate at 4-18°C with the cap screwed on tightly.
- Once the culture is established, follow the protocol for maintenance of culture.
|
| Name of Depositor： |
PG Davis |
| Year of Origin： |
1982 |
| References： |
Wainright PO, et al. Monophyletic origins of the metazoa: an evolutionary link with fungi. Science 260: 340-342, 1993. PubMed: 8469985
Carr M, et al. Molecular phylogeny of choanoflagellates, the sister group to Metazoa. Proc. Natl. Acad. Sci. USA. 105: 16641-16646, 2008. PubMed: 18922774
|
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