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Fibrocystic disease
MCF 10A was derived from adherent cells in the population.
Homo sapiens, human Tissue: Mammary gland; breast Morphology: Epithelial Properties: Adherent Cytogenic data: The MCF 10A cell line is a non-tumorigenic epithelial cell line. The cells are positive for epithelial sialomucins, cytokeratins and milk fat globule antigen. They exhibit three dimensional growth in collagen, and form domes in confluent cultures. Thus far, the cells have shown no signs of terminal differentiation or senescence. The line is responsive to insulin, glucocorticoids, cholera enterotoxin, and epidermal growth factor (EGF). Patient: Female, Caucasian, 36 years of age. Medium: DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Mammary gland; breast Morphology: Epithelial Properties: Adherent Cytogenic data: The MCF 10A cell line is a non-tumorigenic epithelial cell line. The cells are positive for epithelial sialomucins, cytokeratins and milk fat globule antigen. They exhibit three dimensional growth in collagen, and form domes in confluent cultures. Thus far, the cells have shown no signs of terminal differentiation or senescence. The line is responsive to insulin, glucocorticoids, cholera enterotoxin, and epidermal growth factor (EGF). Patient: Female, Caucasian, 36 years of age. Medium: DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Epithelial Properties: Adherent Cytogenic data: The MCF 10A cell line is a non-tumorigenic epithelial cell line. The cells are positive for epithelial sialomucins, cytokeratins and milk fat globule antigen. They exhibit three dimensional growth in collagen, and form domes in confluent cultures. Thus far, the cells have shown no signs of terminal differentiation or senescence. The line is responsive to insulin, glucocorticoids, cholera enterotoxin, and epidermal growth factor (EGF). Patient: Female, Caucasian, 36 years of age. Medium: DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Adherent Cytogenic data: The MCF 10A cell line is a non-tumorigenic epithelial cell line. The cells are positive for epithelial sialomucins, cytokeratins and milk fat globule antigen. They exhibit three dimensional growth in collagen, and form domes in confluent cultures. Thus far, the cells have shown no signs of terminal differentiation or senescence. The line is responsive to insulin, glucocorticoids, cholera enterotoxin, and epidermal growth factor (EGF). Patient: Female, Caucasian, 36 years of age. Medium: DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
The MCF 10A cell line is a non-tumorigenic epithelial cell line. The cells are positive for epithelial sialomucins, cytokeratins and milk fat globule antigen. They exhibit three dimensional growth in collagen, and form domes in confluent cultures. Thus far, the cells have shown no signs of terminal differentiation or senescence. The line is responsive to insulin, glucocorticoids, cholera enterotoxin, and epidermal growth factor (EGF). Patient: Female, Caucasian, 36 years of age. Medium: DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Female, Caucasian, 36 years of age. Medium: DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
DMEM/F12 (1:1) + 5% Horse Serum + EGF (20 ng/mL) + Hydrocortisone (0.5 ug/mL) + Cholera Toxin (100 ng/mL) + Insulin (10ug/mL). Subculture: Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Remove medium, and rinse with 0.05% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 37C. A subcultivation ratio of 1:3 to 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Freezing Medium:70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
70% growth medium supplemented with 10% (v/v) DMSO and 20% horse serum
I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
Amelogenin: X CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
CSF1PO: 10, 12 D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
D13S317: 8, 9 D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
D16S539: 11, 12 D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
D5S818:10, 13 D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
D7S820:10, 11 THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
THO1:8, 9.3 TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
TPOX: 9, 11 vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
vWA: 15, 17 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
If use of this culture results in a scientific publication, it should be cited in the publication as: MCF-10A (AddexBio C0006015)
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