HBEC-5i cells
Catalog #:
T0005011
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Disease:
Normal
Origin:
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.
Species:
Homo sapiens, human
Brain, cerebral cortex
Cerebral microvascular endothelium
Adherent
HBEC-5i cell line has been shown to retain many of the characteristics of endothelial cells. DMEM/F12 + 10% FBS + 40ug/mL endothelial growth supplement (ECGS)
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 37°C 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, 37°C.
Complete growth culture medium supplemented with 7.5% (v/v) DMSO II (Cells contain SV-40 viral DNA sequences)
Bacteria: Negative
Yeast: Negative
Mycoplasma: Negative
HIV: Negative
Hepatitis B: Negative
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
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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Citation Format:
References for HBEC-5i cells:
1. Wassmer SC, de Souza JB, Frère C, Candal FJ, Juhan-Vague I, Grau GE. TGF-beta1 released from activated platelets can induce TNF-stimulated human brain endothelium apoptosis: a new mechanism for microvascular lesion during cerebral malaria. J Immunol. 2006 Jan 15;176(2):1180-1184. PMID: 16394007