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BNL SV A.8
BNL SV A.8
规格:
货期:
编号:TS212571
品牌:Testobio
产品名称: BNL SV A.8
商品货号: TS212571
Organism: Mus musculus, mouse
Tissue: liver
Cell Type: SV40 transformed
Product Format: frozen
Morphology: epithelial
Culture Properties: adherent
Biosafety Level: 2 Cells contain polyomavirus DNA sequences

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: embryo
Strain: BALB/c
Applications:
This line was derived from BNL CL.2 (ATCC TIB-73).
Tested and found negative for ectromelia virus (mousepox).
Storage Conditions: liquid nitrogen vapor phase
Derivation:
This line was derived from BNL CL.2 (ATCC TIB-73).
Tumorigenic: No
Effects:
No, does not form tumors in normal syngeneic mice
Yes, forms tumors in immunodeficient (ATxFL) mice
Comments:
This line was derived from BNL CL.2 (ATCC TIB-73).
The cells will grow in 0.3% agarose.
Tested and found negative for ectromelia virus (mousepox).
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: fetal bovine serum to a final concentration of 10%.
Subculturing:
Protocol:
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that 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).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
  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 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:6 is recommended
Medium Renewal: 2 to 3 times per week
Cryopreservation:
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37.0°C
Name of Depositor: P Patek, J Collins, M Cohn
Deposited As: Mus musculus
References:

Patek PQ, et al. Transformed cell lines susceptible or resistant to in vivo surveillance against tumorigenesis. Nature 276: 510-511, 1978. PubMed: 723934

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BNL SV A.8

  • 货号: TS212571
  • 好评
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  • 品牌 : TESTOBIO
产品名称: BNL SV A.8
商品货号: TS212571
Organism: Mus musculus, mouse
Tissue: liver
Cell Type: SV40 transformed
Product Format: frozen
Morphology: epithelial
Culture Properties: adherent
Biosafety Level: 2 Cells contain polyomavirus DNA sequences

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: embryo
Strain: BALB/c
Applications:
This line was derived from BNL CL.2 (ATCC TIB-73).
Tested and found negative for ectromelia virus (mousepox).
Storage Conditions: liquid nitrogen vapor phase
Derivation:
This line was derived from BNL CL.2 (ATCC TIB-73).
Tumorigenic: No
Effects:
No, does not form tumors in normal syngeneic mice
Yes, forms tumors in immunodeficient (ATxFL) mice
Comments:
This line was derived from BNL CL.2 (ATCC TIB-73).
The cells will grow in 0.3% agarose.
Tested and found negative for ectromelia virus (mousepox).
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: fetal bovine serum to a final concentration of 10%.
Subculturing:
Protocol:
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that 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).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
  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 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:6 is recommended
Medium Renewal: 2 to 3 times per week
Cryopreservation:
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37.0°C
Name of Depositor: P Patek, J Collins, M Cohn
Deposited As: Mus musculus
References:

Patek PQ, et al. Transformed cell lines susceptible or resistant to in vivo surveillance against tumorigenesis. Nature 276: 510-511, 1978. PubMed: 723934

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