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HBEC-5i cells were derived from small fragments of human cerebral cortex obtained from patients who had died of various causes. These brains were devoid of any pathologic abnormalities. Isolation and purification procedures were performed and the cells were cultured. They were then transfected with plasmid containing SV40 large T antigen.
Homo sapiens, human Tissue: Brain, cerebral cortex Morphology: Cerebral microvascular endothelium Properties: Adherent Cytogenic data: HBEC-5i cell line has been shown to retain many of the characteristics of endothelial cells.Medium: DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS) Subculture: Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Brain, cerebral cortex Morphology: Cerebral microvascular endothelium Properties: Adherent Cytogenic data: HBEC-5i cell line has been shown to retain many of the characteristics of endothelial cells.Medium: DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS) Subculture: Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Cerebral microvascular endothelium Properties: Adherent Cytogenic data: HBEC-5i cell line has been shown to retain many of the characteristics of endothelial cells.Medium: DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS) Subculture: Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Adherent Cytogenic data: HBEC-5i cell line has been shown to retain many of the characteristics of endothelial cells.Medium: DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS) Subculture: Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
HBEC-5i cell line has been shown to retain many of the characteristics of endothelial cells.Medium: DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS) Subculture: Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS) Subculture: Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Note: These cells are cultured on vessels coated with 0.1% Gelatin. Use 1.0 mL of gelatin per 10 cm2 surface area. Incubate at 37C for 45 min. Aspirate gelatin just prior to adding cells to vessels. Subculture sub-confluent cultures (70-80%) at 1:4 to 1:10 ratio, using 0.25% (w/v) Trypsin- 0.53 mM EDTA solution. Culture at 5% CO2, 37C. Freezing Medium:Complete growth culture medium supplemented with 7.5% (v/v) DMSO Biosafety Level: II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Complete growth culture medium supplemented with 7.5% (v/v) DMSO
II (Cells contain SV-40 viral DNA sequences) Sterility: Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Bacteria: Negative Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Yeast: Negative Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Mycoplasma: Negative Pathogens: HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
HIV: Negative Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Hepatitis B: Negative DNA Profile (STR): Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
Amelogenin: X, Y CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
CSF1PO: 11, 13 D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
D13S317: 9, 12 D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
D16S539: 10, 13 D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
D5S818: 11, 13 D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
D7S820: 11 THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
THO1:6, 9.3 TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
TPOX: 8, 11 vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
vWA: 14, 18 Citation Format: If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
If use of this culture results in a scientific publication, it should be cited in the publication as: HBEC-5i (AddexBio T0005011)
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