The VEGF mRNA signal is apparent as a dark stain (panel A), and may be compared to the sense control (panel B) which shows no non-specific binding in the same muscle region.

Cytokines and growth factors and their receptors were a major group of IL-1-modulated genes in chondrocytes (Table 2, panel B).

Cytotrophoblast cells associated with small aggregates showed an increase in ERβ immunoreactivity (arrowhead, panel B).

However, in the CL of pregnancy, nuclei of luteal cells show abundant p27 expression (arrow, panel B), accompanied by moderate cytoplasmic staining.

In contrast, dexamethasone treatment of NRP-154 cells did not inhibit IL-6 synthesis; instead dexamethasone treatment apparently enhanced IL-6 production (panel B).

No immunoreactivity was evident suggesting that the staining pattern seen in the chick using the anti-trypsin antibody was specific (figure 3, panel B).

This new complex is specifically induced by the immune antisera since it is not present when the pre-immune serum is used (Figure 1, panel B).

Transcription of treated DNA was initiated from the UV5 (panel A) and N25 (panel B) promotersCT01 and subsequently elongated for 1,5 and 15 min.

As shown in Figure 3, there is a predominant nuclear localization of the hemagglutinin epitope (panel A) compared to the low-level cytoplasmic and nuclear background reactivity seen in the uninduced LLWO2F control cells (panel B).

DNA mobility shift assay using a consensus octamer oligonucleotide and extracts from BHK-21 cells (panel a ) or HeLa cells (panel b ).