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VH 2
VH 2
规格:
货期:
编号:TS210697
品牌:Testobio
产品名称: VH 2
商品货号: TS210697
Organism: Daboia russelii, Russells viper
Tissue: heart
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
Gender: female
Storage Conditions: liquid nitrogen vapor phase
Karyotype: modal number = 35; range = 22 to 67.
Karyotype stable with a near-diploid stemline number. The cells have 16 macrochromosomes and from 17 to 20 microchromosomes.
Virus Susceptibility: Herpes simplex virus
Vaccinia virus
Vesicular stomatitis virus
Human poliovirus 1
Comments: The genus name has been reclassified to Daboia russelii formerly known as Vipera russelii
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Eagles Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
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 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.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 30°C. Atmosphere: Air, 95%; carbon dioxide (CO2), 5%xa0

xa0

Subcultivation Ratio: 1:2
Medium Renewal: Once a week

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:
Complete growth medium 95%; DMSO, 5%.xa0Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:

Temperature: 30°C
Atmosphere: Air, 95%;xa0CO2, 5%

Name of Depositor: HF Clark
Deposited As: Vipera russelli
Year of Origin: June, 1968
References:

. . In Vitro 6: 376, 1971.

Clark HF, et al. Comparative characterization of a C-type virus-producing cell line (VSW) and a virus-free cell line (VH2) from Vipera russelli. J. Natl. Cancer Inst. 51: 645-654, 1973. PubMed: 4358139

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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VH 2

  • 货号: TS210697
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  • 品牌 : TESTOBIO
产品名称: VH 2
商品货号: TS210697
Organism: Daboia russelii, Russells viper
Tissue: heart
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
Gender: female
Storage Conditions: liquid nitrogen vapor phase
Karyotype: modal number = 35; range = 22 to 67.
Karyotype stable with a near-diploid stemline number. The cells have 16 macrochromosomes and from 17 to 20 microchromosomes.
Virus Susceptibility: Herpes simplex virus
Vaccinia virus
Vesicular stomatitis virus
Human poliovirus 1
Comments: The genus name has been reclassified to Daboia russelii formerly known as Vipera russelii
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Eagles Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
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 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.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 30°C. Atmosphere: Air, 95%; carbon dioxide (CO2), 5%xa0

xa0

Subcultivation Ratio: 1:2
Medium Renewal: Once a week

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:
Complete growth medium 95%; DMSO, 5%.xa0Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:

Temperature: 30°C
Atmosphere: Air, 95%;xa0CO2, 5%

Name of Depositor: HF Clark
Deposited As: Vipera russelli
Year of Origin: June, 1968
References:

. . In Vitro 6: 376, 1971.

Clark HF, et al. Comparative characterization of a C-type virus-producing cell line (VSW) and a virus-free cell line (VH2) from Vipera russelli. J. Natl. Cancer Inst. 51: 645-654, 1973. PubMed: 4358139

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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