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Immortalized-Rat-Olfactory-Ensheathing-Glia-SV40

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Immortalized-Rat-Olfactory-Ensheathing-Glia-SV40

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Immortalized-Rat-Olfactory-Ensheathing-Glia-SV40

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	Print Version
BioSafety Level	II
Organism	Rat (P-21)
Source Organ	Nerve fiber layer of rat oflactory bulbs
Growth Properties	Adherent
Morphology	Polygonal
Recommended Seeding Density	Thaw entire contents into an appropriate T25 flask as specified in the Propagation instructions.
Markers	p75-NGFr, Nestin, GFAP, Sulfatide O4
Applications	For Research Use Only
Immortalization Method	Serial passaging and transduction with recombinant lentiviruses carrying SV40 Large T antigen (Plasmid pEF321-T, with EF1α promoter)
Description	Olfactory bulb ensheating glia (OEG) is valued for its unique properties in promoting regeneration of the central nervous system components. The Immortalized Rat Olfactory Ensheating Glia (TEG) maintains its primary characteristics and is useful in biochemical analyses of neuroregenerative mechanisms, as well as in the development of therapeutic protocols for central nervous system regeneration in vivo. When used as a substrate for retinal ganglion neurons (RGN), the Immortalized Rat Olfactory Ensheating Glia (TEG) is effective in promoting neurite outgrowth and regeneration.
Procedure Overview
Image
Propagation	Use of PriCoat? T25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) is required for cell adhesion to the culture vessels. Grow cells in ECM-coated culture vessels with the following conditions. The base medium for this cell line is Prigrow IV medium available from ABM (TM004). To make the complete growth medium, add the following components to the base medium: fetal bovine serum (TM999) to a final concentration of 10%, pituitary extract to 20ug/ml, forskolin to 2uM and Penicillin/Streptomycin(G255). Atmosphere: air: 95%, CO₂: 5%; Temperature: 37.0°C.
Quality Control	Immunohistochemical staining of SV40 T antigen
Reference	Moreno-Flores, M.T., et al. (2003). Immortalized olfactory ensheathing glia promote axonal regeneration of rat retinal ganglion neurons. Journal of Neurochemistry (85): 861–871.
Disclaimer	1. The CoA for this product (provided upon request) verifies the cell-type specific gene expression via RT-PCR only. All test parameters provided in the CoA are conducted using abm's standardized culture system and procedures. The stated values may vary under the end-user's culture conditions. Please verify that the product is suitable for your studies by referencing published papers or ordering RNA (0.5 μg, Cat.# C207, $450.00) or cell lysate (100 μg, Cat.# C206, $600.00) to perform preliminary experiments, or alternatively use our Gene Expression Assay Service (Cat# C138). All sales are final. 2. We strongly recommend live cell shipments for ease of cell transfer and this option can be requested at the time of ordering. Please note that the end-user will need to evaluate the feasibility of live cell shipment by taking into account the final destination's temperature variation and its geographical location. In addition, we thoroughly test our cell lines for freeze-thaw recovery. If frozen cells were received and not recovered in your lab under the exact, specified conditions (using recommended culture vessel, media, additional supplements, and atmospheric conditions), a live cell replacement is possible at a cost (plus shipping). 3. All of abm's cell biology products are for research use ONLY and NOT for therapeutic/diagnostic applications. abm is not liable for any repercussions arising from the use of its cell biology product(s) in therapeutic/diagnostic application(s). Please contact a technical service representative for more information. 4. abm makes no warranties or representations as to the accuracy of the information on this site. Citations from literature and provided for informational purposes only. abm does not warrant that such information has been shown to be accurate.