A new cloning method for antibody-forming lymphoblastoid cells: Increase in cloning efficiency by inclusion of human fibroblasts into semisolid agarose growth layer Journal Article


Authors: Kosinski, S.; Hämmerling, U.
Article Title: A new cloning method for antibody-forming lymphoblastoid cells: Increase in cloning efficiency by inclusion of human fibroblasts into semisolid agarose growth layer
Abstract: We report the development of a method for cloning human EBV-transformed cells which has greater efficiency than techniques used presently. In this new method lymphoblastoid cells are cultured in semisolid agarose in close physical association with human fibroblasts. The results indicate a 10-fold increase in the cloning efficiencies. The average cloning efficiency, depending on the age of cell lines, was from 1 to 14%, and colonies appeared 7-9 days sooner than in the traditional soft agarose method. The new method has allowed us to develop several stable lymphoblastoid cell lines producing antibody cytotoxic to human B lymphocytes. This method may make it more practical to obtain monoclonal human antibodies from lymphoblastoid cell lines which had previously been unstable due to heterogeneity. © 1986.
Keywords: human cell; cell line; in vitro study; cell culture; fibroblast; fibroblasts; lymphocytes; clone cells; culture media; cell transformation, viral; herpesvirus 4, human; clone; sepharose; lymphoblast; human; priority journal; support, u.s. gov't, p.h.s.; antibody producing cell; antibody-producing cells; epstein-barr virus technique; lymphoblastoid cell cloning; monoclonal antibody, human
Journal Title: Journal of Immunological Methods
Volume: 94
Issue: 1-2
ISSN: 0022-1759
Publisher: Elsevier Science, Inc.  
Date Published: 1986-11-20
Start Page: 201
End Page: 208
Language: English
DOI: 10.1016/0022-1759(86)90234-6
PUBMED: 3023491
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 18 August 2021 -- Source: Scopus
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