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SJD.1
SJD.1
规格:
货期:
编号:TS210918
品牌:Testobio
产品名称: SJD.1
商品货号: TS210918
Organism: Danio rerio, zebrafish
Tissue: caudal fin
Cell Type: fibroblast
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
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.

Age: adult
Strain: SJD
Applications:
This strain of zebrafish is used for genetic mapping.
Storage Conditions: liquid nitrogen vapor phase
Derivation:
SJD.1 is a fibroblast cell line derived from amputated caudal fins of an adult zebrafish, strain SJD.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: heat-inactivated fetal bovine serum to a final concentration of 15%.
Subculturing: Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) trypsin- 0.53mM EDTA-0.5% (w/v) polyvinylpyrrolidone solution to remove all traces of serum ,which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA- polyvinylpyrrolidone solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.xa0
  6. Incubate cultures at 28°C.

Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:4 is recommended
Medium Renewal: Every 2 to 3 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

Cryopreservation:
culture medium 95%; DMSO, 5%
Culture Conditions:
Temperature: 28°C
Name of Depositor: BH Paw, LI Zon
References:

Paw BH, Zon LI. Primary fibroblast cell culture. Methods Cell Biol. 59: 39-43, 1999. PubMed: 9891354

Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.

Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988.

Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC.

首页 > 产品中心 > 微生物培养 > 菌株 > null > SJD.1

SJD.1

  • 货号: TS210918
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: SJD.1
商品货号: TS210918
Organism: Danio rerio, zebrafish
Tissue: caudal fin
Cell Type: fibroblast
Product Format: frozen
Morphology: fibroblast
Culture Properties: adherent
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.

Age: adult
Strain: SJD
Applications:
This strain of zebrafish is used for genetic mapping.
Storage Conditions: liquid nitrogen vapor phase
Derivation:
SJD.1 is a fibroblast cell line derived from amputated caudal fins of an adult zebrafish, strain SJD.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: heat-inactivated fetal bovine serum to a final concentration of 15%.
Subculturing: Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) trypsin- 0.53mM EDTA-0.5% (w/v) polyvinylpyrrolidone solution to remove all traces of serum ,which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA- polyvinylpyrrolidone solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.xa0
  6. Incubate cultures at 28°C.

Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:4 is recommended
Medium Renewal: Every 2 to 3 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

Cryopreservation:
culture medium 95%; DMSO, 5%
Culture Conditions:
Temperature: 28°C
Name of Depositor: BH Paw, LI Zon
References:

Paw BH, Zon LI. Primary fibroblast cell culture. Methods Cell Biol. 59: 39-43, 1999. PubMed: 9891354

Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.

Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988.

Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC.

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