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BNL 1ME A.7R.1
BNL 1ME A.7R.1
规格:
货期:
编号:TS212568
品牌:Testobio
产品名称:BNL 1ME A.7R.1
商品货号:TS212568
Organism:Mus musculus, mouse
Tissue:liver
Cell Type:epithelial, chemically transformed
Product Format:frozen
Morphology:epithelial
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:embryo
Strain:BALB/c
Storage Conditions:liquid nitrogen vapor phase
Derivation:

This line was derived from BNL CL.2 (ATCC TIB-73) by transformation with methylcholanthrene epoxide.

Tumorigenic:Yes
Effects:

Yes, forms tumors in BALB/c mice and ATxFL mice

Comments:

This line was derived from BNL CL.2 (ATCC TIB-73) by transformation with methylcholanthrene epoxide.

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:

Volumes are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes.

  1. Remove and discard culture medium.

  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 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 1:3  to 1:8 is recommended

Medium Renewal: 2 to 3 times weekly

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°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

首页 > 产品中心 > 微生物培养 > 菌株 > BNL 1ME A.7R.1 BALB/c小鼠肝上皮恶性转化细胞株 > BNL 1ME A.7R.1

BNL 1ME A.7R.1

  • 货号: TS212568
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称:BNL 1ME A.7R.1
商品货号:TS212568
Organism:Mus musculus, mouse
Tissue:liver
Cell Type:epithelial, chemically transformed
Product Format:frozen
Morphology:epithelial
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:embryo
Strain:BALB/c
Storage Conditions:liquid nitrogen vapor phase
Derivation:

This line was derived from BNL CL.2 (ATCC TIB-73) by transformation with methylcholanthrene epoxide.

Tumorigenic:Yes
Effects:

Yes, forms tumors in BALB/c mice and ATxFL mice

Comments:

This line was derived from BNL CL.2 (ATCC TIB-73) by transformation with methylcholanthrene epoxide.

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:

Volumes are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes.

  1. Remove and discard culture medium.

  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 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 1:3  to 1:8 is recommended

Medium Renewal: 2 to 3 times weekly

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°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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