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SCA-9 clone 15
SCA-9 clone 15
规格:
货期:
编号:TS210941
品牌:Testobio
产品名称： SCA-9 clone 15
商品货号： TS210941
Organism： Mus musculus, mouse
Tissue： submandibular salivary gland
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： Carcinoma
Gender： male
Applications：
The parental line was derived from an undifferentiated carcinoma of the submandibular gland induced by intraglandular injection of 7,12-dimethylbenzaanthracene.
The line produces low levels of several factors (e.
Tested and found negative for ectromelia virus (mousepox).
Storage Conditions： liquid nitrogen vapor phase
Derivation：
The parental line was derived from an undifferentiated carcinoma of the submandibular gland induced by intraglandular injection of 7,12-dimethylbenzaanthracene.
Clinical Data：
male
Genes Expressed：
epidermal growth factor (EGF); nerve growth factor (NGF); renin; peptide hydrolase
Cellular Products：
epidermal growth factor (EGF); nerve growth factor (NGF); renin; peptide hydrolase
Comments：
This is a soft agar clone of the SCA 124-9 cell line.
The parental line was derived from an undifferentiated carcinoma of the submandibular gland induced by intraglandular injection of 7,12-dimethylbenzaanthracene.
The line produces low levels of several factors (e.g., EGF, NGF).
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 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).
    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: 1:3 to 1:4
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：

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: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor： T Barka
Deposited As： Mus musculus
References：

Barka T, et al. Epidermal growth factor, renin, and peptidase in cultured tumor cells of submandibular gland origin. Lab. Invest. 42: 656-662, 1980. PubMed: 6993784

Boylan MO, et al. Cell-specific expression of the glucose-dependent insulinotropic polypeptide gene in a mouse neuroendocrine tumor cell line. J. Biol. Chem. 272: 17438-17443, 1997. PubMed: 9211887

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.

Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online.

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SCA-9 clone 15

  • 货号: TS210941
  • 好评
询价
  • 品牌 : TESTOBIO
产品名称： SCA-9 clone 15
商品货号： TS210941
Organism： Mus musculus, mouse
Tissue： submandibular salivary gland
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： Carcinoma
Gender： male
Applications：
The parental line was derived from an undifferentiated carcinoma of the submandibular gland induced by intraglandular injection of 7,12-dimethylbenzaanthracene.
The line produces low levels of several factors (e.
Tested and found negative for ectromelia virus (mousepox).
Storage Conditions： liquid nitrogen vapor phase
Derivation：
The parental line was derived from an undifferentiated carcinoma of the submandibular gland induced by intraglandular injection of 7,12-dimethylbenzaanthracene.
Clinical Data：
male
Genes Expressed：
epidermal growth factor (EGF); nerve growth factor (NGF); renin; peptide hydrolase
Cellular Products：
epidermal growth factor (EGF); nerve growth factor (NGF); renin; peptide hydrolase
Comments：
This is a soft agar clone of the SCA 124-9 cell line.
The parental line was derived from an undifferentiated carcinoma of the submandibular gland induced by intraglandular injection of 7,12-dimethylbenzaanthracene.
The line produces low levels of several factors (e.g., EGF, NGF).
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 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).
    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: 1:3 to 1:4
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：

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: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor： T Barka
Deposited As： Mus musculus
References：

Barka T, et al. Epidermal growth factor, renin, and peptidase in cultured tumor cells of submandibular gland origin. Lab. Invest. 42: 656-662, 1980. PubMed: 6993784

Boylan MO, et al. Cell-specific expression of the glucose-dependent insulinotropic polypeptide gene in a mouse neuroendocrine tumor cell line. J. Biol. Chem. 272: 17438-17443, 1997. PubMed: 9211887

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.

Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online.

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