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Homo sapiens, human Tissue: Colon Morphology: Epithelial; although FHC cells exhibit epithelial morphology, cytoplasmic keratins were not detected. Properties: Adherent Patient: 13 weeks gestation. Medium: A 1:1 mixture of DMEM:F12 Medium.To make the complete growth medium, add the following components to the base medium: extra 10 mM HEPES (for a final conc. of 25 mM); 10 ng/ml cholera toxin; 0.005 mg/ml insulin; 0.005 mg/ml transferrin; 100 ng/ml hydrocortisone; fetal bovine serum 10% (final conc.) 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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Colon Morphology: Epithelial; although FHC cells exhibit epithelial morphology, cytoplasmic keratins were not detected. Properties: Adherent Patient: 13 weeks gestation. Medium: A 1:1 mixture of DMEM:F12 Medium.To make the complete growth medium, add the following components to the base medium: extra 10 mM HEPES (for a final conc. of 25 mM); 10 ng/ml cholera toxin; 0.005 mg/ml insulin; 0.005 mg/ml transferrin; 100 ng/ml hydrocortisone; fetal bovine serum 10% (final conc.) 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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Epithelial; although FHC cells exhibit epithelial morphology, cytoplasmic keratins were not detected. Properties: Adherent Patient: 13 weeks gestation. Medium: A 1:1 mixture of DMEM:F12 Medium.To make the complete growth medium, add the following components to the base medium: extra 10 mM HEPES (for a final conc. of 25 mM); 10 ng/ml cholera toxin; 0.005 mg/ml insulin; 0.005 mg/ml transferrin; 100 ng/ml hydrocortisone; fetal bovine serum 10% (final conc.) 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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Adherent Patient: 13 weeks gestation. Medium: A 1:1 mixture of DMEM:F12 Medium.To make the complete growth medium, add the following components to the base medium: extra 10 mM HEPES (for a final conc. of 25 mM); 10 ng/ml cholera toxin; 0.005 mg/ml insulin; 0.005 mg/ml transferrin; 100 ng/ml hydrocortisone; fetal bovine serum 10% (final conc.) 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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
13 weeks gestation. Medium: A 1:1 mixture of DMEM:F12 Medium.To make the complete growth medium, add the following components to the base medium: extra 10 mM HEPES (for a final conc. of 25 mM); 10 ng/ml cholera toxin; 0.005 mg/ml insulin; 0.005 mg/ml transferrin; 100 ng/ml hydrocortisone; fetal bovine serum 10% (final conc.) 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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
A 1:1 mixture of DMEM:F12 Medium.To make the complete growth medium, add the following components to the base medium: extra 10 mM HEPES (for a final conc. of 25 mM); 10 ng/ml cholera toxin; 0.005 mg/ml insulin; 0.005 mg/ml transferrin; 100 ng/ml hydrocortisone; fetal bovine serum 10% (final conc.) 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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
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 1:2 to 1:4 is recommended every 10-15 days. Renew medium once every 3 to 4 days depending on cell density. Freezing Medium:Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO Biosafety Level: I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Complete growth medium supplemented with an extra 50% FBS and 10% (v/v) DMSO
I Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
Amelogenin: X, Y CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
CSF1PO: 11, 12 D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
D13S317: 12, 13 D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
D16S539: 9, 11 D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
D5S818:12, 13 D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
D7S820: 8, 12 THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
THO1:6, 9.3 TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
TPOX: 8, 11 vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
vWA: 16 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
If use of this culture results in a scientific publication, it should be cited in the publication as: FHC (AddexBio P0009022)
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