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FT
FT
规格:
货期:
编号:TS212139
品牌:Testobio
产品名称: FT
商品货号: TS212139
Organism: Rana catesbelana, bullfrog
Tissue: tongue, normal
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.

Disease: normal
Age: adult
Gender: female
Storage Conditions: liquid nitrogen vapor phase
Karyotype: modal number = 43; range = 36 to 49
Interesting extended centromeric region in chromosomes of many cells; chromosomes are large; some chromosomes have the secondary constrictions found in diploid cells. Karyotype of stemline cells unstable.
Clinical Data:
female
Virus Resistance:
poliovirus 1; herpes simplex; adenovirus 3; vesicular stomatitis (Indiana); infectious pancreatic necrosis virus of trout
Complete Growth Medium: Minimum essential medium (Eagle) with 2 mM L-glutamine and Earles BSS adjusted to contain 1.5 g/L sodium bicarbonate, 0.1 mM non-essential amino acids, and 1.0 mM sodium pyruvate supplemented with 10% double distilled water and 10% fetal bovine serum.
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 cold 0.25% (w/v) Trypsin-0.53mMxa0 EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA 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.xa0
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 25°C.

Subcultivation Ratio: 1:2 to 1:3
Medium Renewal: Two to three times weekly

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.xa0xa0

Cryopreservation:

Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:
Temperature: 25°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor: K Wolf
Deposited As: Rana catesbelana
Year of Origin: July, 1961
References:

Wolf K, Quimby MC. Amphibian cell culture: permanent cell line from the bullfrog (Rana catesbeiana). Science 144: 1578-1580, 1964. PubMed: 14169344

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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FT

  • 货号: TS212139
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称: FT
商品货号: TS212139
Organism: Rana catesbelana, bullfrog
Tissue: tongue, normal
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.

Disease: normal
Age: adult
Gender: female
Storage Conditions: liquid nitrogen vapor phase
Karyotype: modal number = 43; range = 36 to 49
Interesting extended centromeric region in chromosomes of many cells; chromosomes are large; some chromosomes have the secondary constrictions found in diploid cells. Karyotype of stemline cells unstable.
Clinical Data:
female
Virus Resistance:
poliovirus 1; herpes simplex; adenovirus 3; vesicular stomatitis (Indiana); infectious pancreatic necrosis virus of trout
Complete Growth Medium: Minimum essential medium (Eagle) with 2 mM L-glutamine and Earles BSS adjusted to contain 1.5 g/L sodium bicarbonate, 0.1 mM non-essential amino acids, and 1.0 mM sodium pyruvate supplemented with 10% double distilled water and 10% fetal bovine serum.
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 cold 0.25% (w/v) Trypsin-0.53mMxa0 EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA 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.xa0
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 25°C.

Subcultivation Ratio: 1:2 to 1:3
Medium Renewal: Two to three times weekly

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.xa0xa0

Cryopreservation:

Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:
Temperature: 25°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor: K Wolf
Deposited As: Rana catesbelana
Year of Origin: July, 1961
References:

Wolf K, Quimby MC. Amphibian cell culture: permanent cell line from the bullfrog (Rana catesbeiana). Science 144: 1578-1580, 1964. PubMed: 14169344

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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