|Supplied by:||European Collection of Authenticated Cell Cultures (ECACC)|
|Culture Type:||Cell line, hybridoma|
|Collection:||ECACC Hybridoma Collection|
|Cell Line Name:||IC-01|
|Other Collection No.:||ATCC N/A|
|Reactivity:||Anti- galactocerebroside, monoglactosyldiglyceride psychosine|
|Fusion Species:||Mouse x Mouse Hybridoma|
|Immunological Donor:||BALB/c mouse spleen|
|Immunogen:||Particulate fraction from bovine corpus callosum|
|Transfected DNA:||Not Applicable|
|Cell Line Description:||The antibody is directed against galactocerebroside monogalactosyldiglyceride and psychosine. It will react with oligodendrocytes and Schwann cells in cattle, rodents, chick and fish.|
|Citation Guidance:||If use of this culture results in a scientific publication, it should be cited in the publication as: IC-01 (ECACC 93042001)|
|Sub Culture Routine:||
Maintain cultures between 3-9x100,000 cells/ml; 5% CO2; 37°C.
When recovering hybridoma cultures from frozen it is not unusual for growth to be slower than expected initially and there may be an observed decrease in viability. Establishment of an actively proliferating culture may take up to 2 weeks.
On resuscitation a centrifugation step to remove the cryoprotectant is essential. Rapidly thaw the frozen ampoule in a water bath at 37°C for 1-2 minutes. Transfer the contents to a centrifuge tube and slowly add 5-10ml of prewarmed growth media+. Remove a sample for counting. Centrifuge at 100 x g for 2-3 minutes to pellet cells and seed at a relatively high density of 5-7 x 10⁵ cells/ml. Place culture flask flat and observe regularly until viable proliferating cells are seen.
Often hybridoma cultures may benefit from being resuspended with media supplemented with 20% FBS in the early critical stage of culture establishment immediately post resuscitation. Once the culture is established in culture the FBS can be reduced to 10%.
|Culture Medium:||DMEM + 2mM glutamine + 10% Foetal Bovine Serum (FBS)|
|Depositor:||Dr I Sommer, Dept. of Neurology, University of Glasgow|
|References:||Dev Biol 1981;83:311; Dev Brain Res 1987;35:249|
|Patent:||None Specified by Depositor|
|Hazard Group (ACDP):||1|
Unless specified otherwise, at the European Collection of Authenticated Cell Cultures (ECACC) we routinely handle all of our cell lines at containment level 2 in accordance with the ACDP guidelines. ACDP = Advisory Committee on Dangerous Pathogens (UK)
All cell cultures have the potential to carry as yet unidentified adventitious agents. It is the responsibility of the end user to ensure that their facilities comply with biosafety regulations for their own country.
ACDP Guidance: Biological agents: Managing the risks in laboratories and healthcare premises.
Hyperlinks to MSDS documents:
Frozen cell cultures Material Safety Data Sheet
Growing cell cultures Material Safety Data Sheet
Nucleic acids derived from cell cultures Material Safety Data Sheet
The Culture Collections represent deposits of cultures from world-wide sources. While every effort is made to ensure details distributed by Culture Collections are accurate, Culture Collections cannot be held responsible for any inaccuracies in the data supplied. References where quoted are mainly attributed to the establishment of the cell culture and not for any specific property of the cell line, therefore further references should be obtained regarding cell culture characteristics. Passage numbers where given act only as a guide and Culture Collections does not guarantee the passage number stated will be the passage number received by the customer.
Cultures supplied by Culture Collections are for research purposes only. Enquiries regarding the commercial use of a cell line are referred to the depositor of the cell line. Some cell lines have additional special release conditions such as the requirement for a material transfer agreement to be completed by the potential recipient prior to the supply of the cell line. Please view the Terms & Conditions of Supply for more information.
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