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Human Oligodendrocytes
(HO)
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| Catalog Number: 1620 |
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Cell Specification
Oligodendrocytes, the myelin-forming cells of the central nervous
system, are postmitotic cells that develop from oligodendrocyte
precursor cells [1]. Oligodendrocytes, through their ability to
myelinate axons, play an essential role in the mature nervous
system [2]. Although the function of oligodendrocytes is well
understood in rodent nervous system, little is known about the
human origin of this cell type. The study of human oligodendrocyte
biology and the treatment of white matter diseases would be facilitated
by the ability to maintain cultures of enriched human oligodendrocytes
or their progenitors [3].
HO from ScienCell Research Laboratories are derived from the
differentiation of HOPC which isolated from human brain tissue.
HO are cryopreserved immediately after purification from HOPC
cultures and delivered frozen. Each vial contains >1 x 106
cells in 1 ml volume. HO are characterized by immunofluorescent
method with antibodies to GalC and CNPase. HO are negative for
HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HO are
guaranteed to further culture in the conditions specified by ScienCell
Research Laboratories.
Recommended Medium
It is recommended to use Oligodendrocyte Medium (OM, Cat.
No. 1621) for the culturing of human oligodendrocyte in
vitro.
Product Use
HO are for research use only. They are not approved for human
or animal use, or for application in in vitro diagnostic
procedures.
Storage
Transfer cells directly and immediately from dry ice to liquid
nitrogen upon receiving and keep the cells in liquid nitrogen
until cell culture is needed for experiments.
Shipping
Dry ice.
Reference
[1] Zhang, S.-C., Ge, B. and Duncan, I. D. (2000) Tracing human
oligodendroglial development in vitro. J. Neurosci. Res. 59:421-429.
[2] Woodruff, R. H. and Franklin, R. J. M. (1997) Growth factors
and remyelination in the CNS. Histol. Histopathol. 12:459-466.
[3] Grever, W. E., Zhang, S.-C., Ge, B. and Duncan, I. D. (1999)
Fractionation and enrichment of oligodendrocytes from developing
human brain. J. Neurosci. Res. 57:304-314.