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Leptomonas podlipaevi
Leptomonas podlipaevi
规格:
货期:
编号:TS181423
品牌:Testobio
产品名称： Leptomonas podlipaevi
商品货号： TS181423
Deposited As： Leptomonas podlipaevi
Strain Designations： clone 5-10-2
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： Heteropteran bug (Boisea rubrolineata), Riverside, California, USA
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
Comments： Intestinal parasite/commensal in Heteroptera
Medium： ATCC® Medium 44: Brain Heart Infusion Agar/Broth
Growth Conditions：
Temperature: 20°C to 25°C
Cryopreservation： Harvest and Preservation
  1. Harvest cells from a culture which is at or near peak density by centrifugation at ~800 x g for 5 min.
  2. Adjust concentration of cells to 2 x 107/mL in fresh medium. xa0If the concentration is too low, centrifuge at ~800 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
  3. While cells are centrifuging, prepare a 10% (v/v) solution of sterile DMSO in fresh medium (broth).xa0 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.
  4. Mix the cell preparation and the DMSO solution in equal portions. The final concentration will be 107 cells/mL and 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 more 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 ampules 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 If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion.xa0 At -40°C, plunge ampules into liquid nitrogen.
  7. Store in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To thaw a frozen ampule, place it in a 35°C water bath such that the lip of the ampule remains above the water line. Thawing time is approximately 2 to 3 minutes.xa0 Do not agitate the ampule.xa0 Do not leave ampule in water bath after it is thawed.
  9. Remove the vial from the water bath immediately after thawing.xa0 Aseptically transfer the contents of the ampule into a T-25 tissue culture flask containing 10.0 mL ATCC medium 44 supplemented with 10 μg/mL hemin.xa0
  10. Incubate the tube at 20-25°C with the cap screwed on tightly.
  11. Maintain as described above.
Name of Depositor： D Maslov
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Leptomonas podlipaevi

  • 货号: TS181423
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称： Leptomonas podlipaevi
商品货号： TS181423
Deposited As： Leptomonas podlipaevi
Strain Designations： clone 5-10-2
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： Heteropteran bug (Boisea rubrolineata), Riverside, California, USA
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
Comments： Intestinal parasite/commensal in Heteroptera
Medium： ATCC® Medium 44: Brain Heart Infusion Agar/Broth
Growth Conditions：
Temperature: 20°C to 25°C
Cryopreservation： Harvest and Preservation
  1. Harvest cells from a culture which is at or near peak density by centrifugation at ~800 x g for 5 min.
  2. Adjust concentration of cells to 2 x 107/mL in fresh medium. xa0If the concentration is too low, centrifuge at ~800 x g for 5 minutes and resuspend the cell pellet with a volume of supernatant to yield the desired concentration.
  3. While cells are centrifuging, prepare a 10% (v/v) solution of sterile DMSO in fresh medium (broth).xa0 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.
  4. Mix the cell preparation and the DMSO solution in equal portions. The final concentration will be 107 cells/mL and 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 more 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 ampules 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 If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion.xa0 At -40°C, plunge ampules into liquid nitrogen.
  7. Store in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To thaw a frozen ampule, place it in a 35°C water bath such that the lip of the ampule remains above the water line. Thawing time is approximately 2 to 3 minutes.xa0 Do not agitate the ampule.xa0 Do not leave ampule in water bath after it is thawed.
  9. Remove the vial from the water bath immediately after thawing.xa0 Aseptically transfer the contents of the ampule into a T-25 tissue culture flask containing 10.0 mL ATCC medium 44 supplemented with 10 μg/mL hemin.xa0
  10. Incubate the tube at 20-25°C with the cap screwed on tightly.
  11. Maintain as described above.
Name of Depositor： D Maslov
testopic
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