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Osteoblast; SV40 large T antigen transfected
This line was established by transfection of limb tissue obtained from a spontaneous miscarriage with the temperature sensitive expression vector pUCSVtsA58 and the neomycin resistance expression vector pSV2-neo. Clones were selected in the presence of 0.6 mg/mL G418.
Homo sapiens, human Tissue: Bone Morphology: Osteoblast Properties: Adherent Cytogenic data: diploid, 43%; tetraploid, 57%. Patient: Fetus. Medium: 1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Bone Morphology: Osteoblast Properties: Adherent Cytogenic data: diploid, 43%; tetraploid, 57%. Patient: Fetus. Medium: 1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Osteoblast Properties: Adherent Cytogenic data: diploid, 43%; tetraploid, 57%. Patient: Fetus. Medium: 1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Adherent Cytogenic data: diploid, 43%; tetraploid, 57%. Patient: Fetus. Medium: 1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
diploid, 43%; tetraploid, 57%. Patient: Fetus. Medium: 1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Fetus. Medium: 1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
1:1 mixture of Ham's F12 Medium Dulbecco's Modified Eagle's Medium, with 2.5 mM L-glutamine (without phenol red) + 10% FBS + G418 (0.3 mg/mL) Subculture: Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Remove medium, and rinse with 0.05% trypsin, 0.03 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 34C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks. Culture at 5% CO2, 34C. A subcultivation ratio of 1:4 is recommended. Renew medium once every 2 to 3 days depending on cell density. Cells grown at a permissive temperature of 33.5C exhibit rapid cell division (Doubling time of 36 hrs), whereas little cell division occurs at a restrictive temperature of 39.5C (Doubling time of 96 hrs). The cells have the ability to differentiate into mature osteoblasts expressing the normal osteoblast phenotype. At the restrictive temperatures, cell division is slowed, differentiation increases, and a more mature osteoblast phenotype is produced. Freezing Medium:Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8% Biosafety Level: II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Culture medium, 72%; additional fetal bovine serum, 20%; DMSO, 8%
II [Cells contain SV40 viral sequences] Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Hepatitis B: Negative DNA Profile (STR): Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
Amelogenin: X CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
CSF1PO: 10, 13 D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
D13S317: 11, 12 D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
D16S539: 9, 13 D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
D5S818:11, 12 D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
D7S820:8, 10 THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
THO1:7, 9.3 TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
TPOX: 11 vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
vWA: 16, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
If use of this culture results in a scientific publication, it should be cited in the publication as: hFOB1.19 (AddexBio T0004005)
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