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C1

C1

Catalogue No.

99061825

Cell Line Name

C1

Cell Line Description

The hybridoma C1 was produced from a (C57Bl/6xBALB/c)F1 mouse immunised with a single i.p. injection of the lymphoblastoid cell line Co and Bordetella pertussis organisms. The B cell line Co was expressing HLA A1, B8, C7, DR3 and DQ2. The mouse spleen was removed 3 days after immunisation and fused with the myeloma P3x63Ag8.653. C1 monoclonal antibodies were shown to react with cells expressing the class II antigen DQw2. The hybridoma is also known as COX IA2. C1 has been analysed in the International Histocompatibility Workshop 10 (IOW3105) and 12 (12W593).

Characteristics

Myeloma

P3X63 Ag8.653

Immunogen

B cell line Co, HLA A1,B8 C7, DR3,DQ2

Immunological Donor

(C57BL/6 x BALB/c)F1

Antibody Isotype

IgM

Morphology

Spherical

Tissue of Origin

Hybrid

Culture Conditions

Cell Type

Hybridoma

Subculture Routine

Maintain cultures between 3-9 x 100,000 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 10µ 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

RPMI 1640 + 2mM glutamine + 1mM NaP + 10% FBS

Growth Mode

Suspension

Additional Info

Depositor

Dr. JP Johnson, Institute for Immunology, Goethestrasse 31, 80336, Munich, Germany

Country of Origin

Germany

Applications

Immunofluorescence, cytotoxicity

Assays

Cell ELISA on HLA typed lymphoblastoid cell lines

Hazard Group (ACDP)

2

References

References

Tissue Antigens 1987; 29:26

Available Formats

  • Frozen

If use of this culture results in a scientific publication, it should be cited in the publication as: C1 (ECACC 99061825)

Unless specified otherwise, at ECACC we routinely handle all of our cell lines at containment level 2 in accordance with the ACDP guidelines (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.

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.