Abstract
Modification of antibody effector functions is commonly performed by chimerization or humanization. Cloning of antibody variable regions from hybridomas represents a first step that is frequently hampered by the expression of non-functionally rearranged variable regions in hybridoma cells that originate from MOPC21-derived fusion partners. We now present a simple method to clone functionally rearranged V-genes, based on V-gene-specific multiplex PCR screening. Using this method we document the expression of aberrant V-genes that originate from the original B-cell used for the hybridoma generation, not from the fusion partner, and are - thus - hybridoma specific
| Original language | English |
|---|---|
| Pages (from-to) | 245-252 |
| Journal | Journal of immunological methods |
| Volume | 249 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 2001 |
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