NMU

规格:

货期:

编号:TS211212

品牌:Testobio

产品名称：	NMU
商品货号：	TS211212
Organism：	Rattus norvegicus, rat
Tissue：	mammary gland
Cell Type：	chemically induced
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：	adenocarcinoma
Age：	50 days adult
Gender：	female
Strain：	Sprague-Dawley
Applications：	The cells synthesize and secrete plasminogen activator, synthesize type IV collagen and produce and secrete nanogram quantities of prostaglandins under defined culture conditions. The cells lack vimentin and react strongly with anti keratin antibodies (evidence of epithelial origin). The cells exhibit the polygonal appearance typical of epithelial cells and develop multicellular domes in confluent cultures.
Storage Conditions：	liquid nitrogen vapor phase
Clinical Data：	female
Receptor Expression：	androgen receptor, positive; glucocorticoid; insulin
Genes Expressed：	collagen (Type IV); plasminogen activator; prostaglandins; keratin
Cellular Products：	collagen (Type IV); plasminogen activator; prostaglandins; keratin
Tumorigenic：	Yes
Effects：	Yes, in newborn Sprague-Dawley rats
Comments：	The cells synthesize and secrete plasminogen activator, synthesize type IV collagen and produce and secrete nanogram quantities of prostaglandins under defined culture conditions. The cells lack vimentin and react strongly with anti keratin antibodies (evidence of epithelial origin). The cells exhibit the polygonal appearance typical of epithelial cells and develop multicellular domes in confluent cultures.
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. Remove and discard culture medium. 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. 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. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting. Add appropriate aliquots of the cell suspension to new culture vessels. Incubate cultures at 37°C. Subcultivation Ratio: 1:2 to 1:6 Medium Renewal: Two times 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 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%
Population Doubling Time：	18 to 20 hrs
Name of Depositor：	LA Cohen
Deposited As：	Rattus sp.
References：	Cohen LA. Isolation and characterization of a serially cultivated, neoplastic, epithelial cell line from the N-nitrosomethylurea induced rat mammary adenocarcinoma. In Vitro 18: 565-575, 1982. PubMed: 7118137 Cohen LA, Karmali RA. Endogenous prostaglandin production by established cultures of neoplastic rat mammary epithelial cells. In Vitro 20: 119-126, 1984. PubMed: 6423517 Vignon F, et al. Hormonal regulation in two rat mammary cancer cell lines: glucocorticoid and androgen receptors. Mol. Cell. Endocrinol. 13: 191-202, 1979. PubMed: 109329 Okazaki IJ, et al. Cloning and characterization of a novel membrane-associated lymphocyte NAD:arginine ADP-ribosyltransferase. J. Biol. Chem. 271: 22052-22057, 1996. PubMed: 8703012 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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NMU

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产品名称：	NMU
商品货号：	TS211212
Organism：	Rattus norvegicus, rat
Tissue：	mammary gland
Cell Type：	chemically induced
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：	adenocarcinoma
Age：	50 days adult
Gender：	female
Strain：	Sprague-Dawley
Applications：	The cells synthesize and secrete plasminogen activator, synthesize type IV collagen and produce and secrete nanogram quantities of prostaglandins under defined culture conditions. The cells lack vimentin and react strongly with anti keratin antibodies (evidence of epithelial origin). The cells exhibit the polygonal appearance typical of epithelial cells and develop multicellular domes in confluent cultures.
Storage Conditions：	liquid nitrogen vapor phase
Clinical Data：	female
Receptor Expression：	androgen receptor, positive; glucocorticoid; insulin
Genes Expressed：	collagen (Type IV); plasminogen activator; prostaglandins; keratin
Cellular Products：	collagen (Type IV); plasminogen activator; prostaglandins; keratin
Tumorigenic：	Yes
Effects：	Yes, in newborn Sprague-Dawley rats
Comments：	The cells synthesize and secrete plasminogen activator, synthesize type IV collagen and produce and secrete nanogram quantities of prostaglandins under defined culture conditions. The cells lack vimentin and react strongly with anti keratin antibodies (evidence of epithelial origin). The cells exhibit the polygonal appearance typical of epithelial cells and develop multicellular domes in confluent cultures.
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. Remove and discard culture medium. 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. 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. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting. Add appropriate aliquots of the cell suspension to new culture vessels. Incubate cultures at 37°C. Subcultivation Ratio: 1:2 to 1:6 Medium Renewal: Two times 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 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%
Population Doubling Time：	18 to 20 hrs
Name of Depositor：	LA Cohen
Deposited As：	Rattus sp.
References：	Cohen LA. Isolation and characterization of a serially cultivated, neoplastic, epithelial cell line from the N-nitrosomethylurea induced rat mammary adenocarcinoma. In Vitro 18: 565-575, 1982. PubMed: 7118137 Cohen LA, Karmali RA. Endogenous prostaglandin production by established cultures of neoplastic rat mammary epithelial cells. In Vitro 20: 119-126, 1984. PubMed: 6423517 Vignon F, et al. Hormonal regulation in two rat mammary cancer cell lines: glucocorticoid and androgen receptors. Mol. Cell. Endocrinol. 13: 191-202, 1979. PubMed: 109329 Okazaki IJ, et al. Cloning and characterization of a novel membrane-associated lymphocyte NAD:arginine ADP-ribosyltransferase. J. Biol. Chem. 271: 22052-22057, 1996. PubMed: 8703012 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.