Abstract

Membrane expression of Fc receptors (FcR) was studied in clones of human K562 cells during short- and long-term culture. Using a manual cloning method, well-defined clones were generated either from FcR-positive or FcR-negative cells. The fourth day after cloning, the majority of cloned cells manifested shifts in FcR expression without evidence of an orderly pattern. After long-term culture (about 34 passages), most clones expressed FcR values close to those found in the cell line. In addition, the selection of six clones expressing a stable FcR phenotype suggested that the presence of FcR is correlated to a low hemoglobinization of the multipotential K562 cells.

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