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平臺編號：bio-086778
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國際編號：ATCC 30388
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拉丁屬名： Tetrahymena thermophila
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規(guī)格：test tube
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用途：ATCC原裝進口
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服務費用：
加載中…… - 訂購
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注意事項：僅用于科學研究或者工業(yè)應用等非醫(yī)療目的不可用于人類或動物的臨床診斷或治療，非藥用，非食用（產品信息以出庫為準）
B3-3686a
Tetrahymena thermophila Nanney and McCoy
(ATCC? 30388?)
Strain Designations B3-3686a
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 derived from B(17) (an F17 derivation of WH-6 and WH-14) X C(16) (an F16 derivation of B(2), an F2 derivation of WH-6 and WH-14, and UM-266) by genomic exclusion, Urbana, IL, 1968
Product Format test tube
Type Strain no
Genotype BEABCBFSSF
Comments derived from B(17) (an F17 derivation of WH-6 and WH-14) X C(16) (an F16 derivation of B(2), an F2 derivation of WH-6 and WH-14, and UM-266) by genomic exclusion, Urbana, IL, 1968
One of a set of related inbred stocks. Designations provide information about the history and mating type. For example, strain A-17682a has the mating type allele A, is the 17th generation of inbreeding, the last inbreeding cross was made in 1968, and this line is mating type II (2). The lower case letter (a) indicates that more than one line of the particular mating type was kept from the cross, and the letter identifies the line.
Medium ATCC? Medium 357: Tetrahymena medium
ATCC? Medium 357: Tetrahymena medium
ATCC? Medium 383: Haskins agar for Tetrahymena
Growth Conditions
Max Temperature: 25.0°C
Min Temperature: 18.0°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
) 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) 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.
9. 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) 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). 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.
Name of Depositor EM Simon, DL Nanney
Chain of Custody ATCC <<--EM Simon, DL Nanney<<--S.L. Allen
Year of Origin 1968
References Borden D, et al. The inheritance of enzyme variants for tyrosine aminotransferase, NADP dependent malate dehydrogenase, NADP dependent isocitrate dehydrogenase and tetrazolium oxidase in Tetrahymena pyriformis syngen 1. Genetics 74: 595-603, 1974.
(ATCC? 30388?)
Strain Designations B3-3686a
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 derived from B(17) (an F17 derivation of WH-6 and WH-14) X C(16) (an F16 derivation of B(2), an F2 derivation of WH-6 and WH-14, and UM-266) by genomic exclusion, Urbana, IL, 1968
Product Format test tube
Type Strain no
Genotype BEABCBFSSF
Comments derived from B(17) (an F17 derivation of WH-6 and WH-14) X C(16) (an F16 derivation of B(2), an F2 derivation of WH-6 and WH-14, and UM-266) by genomic exclusion, Urbana, IL, 1968
One of a set of related inbred stocks. Designations provide information about the history and mating type. For example, strain A-17682a has the mating type allele A, is the 17th generation of inbreeding, the last inbreeding cross was made in 1968, and this line is mating type II (2). The lower case letter (a) indicates that more than one line of the particular mating type was kept from the cross, and the letter identifies the line.
Medium ATCC? Medium 357: Tetrahymena medium
ATCC? Medium 357: Tetrahymena medium
ATCC? Medium 383: Haskins agar for Tetrahymena
Growth Conditions
Max Temperature: 25.0°C
Min Temperature: 18.0°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
) sterilesolution 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
) 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.
9. 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
) 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
). 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.
Name of Depositor EM Simon, DL Nanney
Chain of Custody ATCC <<--EM Simon, DL Nanney<<--S.L. Allen
Year of Origin 1968
References Borden D, et al. The inheritance of enzyme variants for tyrosine aminotransferase, NADP dependent malate dehydrogenase, NADP dependent isocitrate dehydrogenase and tetrazolium oxidase in Tetrahymena pyriformis syngen 1. Genetics 74: 595-603, 1974.
