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Tetrahymena nanneyi Simon et al.拉丁名

(ATCC? 50071?)統(tǒng)一編號(hào)

Strain Designations 菌種別名 LB2 

Biosafety Level 生物安全等級(jí) 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 Lake Beatrice, Elgin, IL, 1971 

Product Format 提供形式 test tube 

Type Strain 模式菌種 yes 

Comments I species description

Medium 培養(yǎng)基 ATCC? Medium 357: Tetrahymena medium 

Growth Conditions 生長條件

Temperature 培養(yǎng)溫度: 25.0°C 

Duration: axenic 

Cryopreservation RM-9 Media for cryopreservation of Tetrahymena 

Proteose Peptone (Difco 0120)     5.0 g

 Tryptone          5.0 g 

 K2HPO4           0.2 g

 Glucose          1.0 g

Liver extract       0.1 g

Glass distilled water     1.0 L 

Dissolve components in glass distilled H2O and autoclave. Dryl’s Salt Solution

0.1 M NaH2PO4 .  3H20  10.0 ml 

0.1 M Na2HPO4 .  7H20  10.0 ml 

0.1 M Sodium citrate . 2H20        15.0 ml 

0.1 M CaCl2 .  2H20             15.0 ml 

Distilled water                950.0 ml 

Add the first 3 components to the distilled H2O and mix thoroughly. Add the CaC12 solution and mix thoroughly. 

 (Adding the solutions in the order indicated will avoid the precipitation of Ca salts.) 

 1.  Transfer tetrahymena from usual growth medium to RM-9 medium and allow to grow to near peak density. 

 2.   Harvest cells from a culture by centrifugation at 300 x g for 2 min.          

 3.   Adjust concentration of cells to 2 x 106/ml in fresh medium. 

 4.   While cells are centrifuging, prepare a 22% (v/v) sterile solution of sterile DMSO in fresh medium. a) Add 2.2 ml of DMSO to an ice cold 20 x 150 mm screw-capped test tube; b) Place the tube on ice and allow the DMSO to solidify (~5 min) and then add 7.8 ml of ice cold medium; c) Invert several times to dissolve the DMSO; d) Allow to warm to room temperature.

5.   Add a volume of the DMSO solution equal to the cell suspension volume but add in 3 equal aliquots at 2 min      intervals. Thus, the final concentration of the preparation will equal 11% (v/v) DMSO and 106 cells /ml. 

6.   Dispense in 0.5 ml aliquots into 1.0 - 2.0 ml sterile plastic screw-capped cryules (special plastic vials for       cryopreservation). 

7.   Place the ampules in a controlled rate freezing unit. The cooling cycle should be initiated no less than 15 min and no longer than 60 min after the addition of the DMSO to the cell preparation. 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  -50°C ampules are plunged into liquid nitrogen. 

8.   Store in the vapor or liquid phase of a nitrogen  refrigerator. 

.   To establish a culture from the frozen state aseptically add 0.5 ml sterile Dryl's Salt Solution to an ampule. Immediately place the ampule in a 35°C water bath, until thawed (2-3 min).  Immerse the ampule just sufficient to cover the frozen material. Do not agitate the ampule. 10. Immediately after thawing, aseptically remove the contents of the ampule and inoculate into 5.0 ml of fresh medium in a 16 x 125 mm screw-capped test tube with a slightly loosened cap. Incubate at 25°C.  

CRYOPRESERVATION: 

 Alternative Thawing Procedure 

1.  Aseptically  add 0.5 ml of sterile modified PYNFH medium (ATCC Medium 1034) containing 8% (w/v) sucrose to the ampule.  Immediately, place in a 35°C water bath, until thawed. Immerse the ampule just sufficient to cover the frozen material. Do not agitate the ampule. 

2.   Immediately after thawing, aseptically remove the contents of the ampule and gently add the material to the edge of a 20 x 100 mm petri plate containing ATCC Medium 919 (non-nutrient agar) and position on a 15 degree slant.  The cell suspension will pool at the edge of the plate. 

3.   Continue to double the volume of the cell suspension at 10 minute intervals by adding ATCC medium 1034) containing 4% sucrose (w/v).  When the volume reaches 16.0 ml place the plate in horizontal position and incubate at 25°C. 

4.   On the following day, gently remove the cell suspension for the plate and transfer to a T-25 tissue culture flask.  Note the volume of the suspension and add a volume of fresh medium containing 4% sucrose equal to the volume of  the cell suspension.  Incubate the culture at 25°C. 

5.   After culture has been established subculture into fresh  normal medium without sucrose.