Fig. 4.
Fig. 4. Subcellular localization of the BAL protein. / (A) Fluorescence microscopy of NIH3T3 fibroblasts transfected with an expression vector encoding GFP alone (left) or GFP-BAL (right). Whereas fibroblasts transfected with GFP alone exhibit diffuse primarily cytoplasmic GFP (left), cells transfected with GFP-BAL exhibit mainly nuclear fluorescence. (B) Western blot analysis of subcellular fractions from aggressive B-cell lymphoma transfectants expressing either GFP alone or GFP-BAL. Cytoplasmic and nuclear cell fractions were blotted and probed with GFP antiserum (left panel) or control antibodies directed against known cytoplasmic (αtubulin, right lower panel) and nuclear (retinoblastoma [Rb], right upper panel) proteins. In these B-cell transfectants, GFP alone (approximately 26 kd) was primarily detected in the cytoplasm whereas GFP-BAL (approximately 114 kd) was predominantly found in the nucleus.

Subcellular localization of the BAL protein.

(A) Fluorescence microscopy of NIH3T3 fibroblasts transfected with an expression vector encoding GFP alone (left) or GFP-BAL (right). Whereas fibroblasts transfected with GFP alone exhibit diffuse primarily cytoplasmic GFP (left), cells transfected with GFP-BAL exhibit mainly nuclear fluorescence. (B) Western blot analysis of subcellular fractions from aggressive B-cell lymphoma transfectants expressing either GFP alone or GFP-BAL. Cytoplasmic and nuclear cell fractions were blotted and probed with GFP antiserum (left panel) or control antibodies directed against known cytoplasmic (αtubulin, right lower panel) and nuclear (retinoblastoma [Rb], right upper panel) proteins. In these B-cell transfectants, GFP alone (approximately 26 kd) was primarily detected in the cytoplasm whereas GFP-BAL (approximately 114 kd) was predominantly found in the nucleus.

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