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Protein phosphorylation and expression were analysed by immunoblotting (images with black bands) (a) and quantified (b).

Protein phosphorylation and expression were analysed by immunoblotting (c,g) and quantified by densitometry (d,h).

The changes in the pattern of gene expression were analysed by means of DNA/RNA hybrid antibodies in the polytene chromosomes from salivary gland cells.

The relative changes in gene expression were analysed by the 2−ΔΔCT method [57].

In order to address if inhibition of transcription would affect the expression of spindle checkpoint transcripts, bubR1, bub3, mad1, mad2 and cdc20 gene expression were analysed by real-time quantitative PCR.

Levels of protein expression were analysed by western-blot.

The relative gene expression was analysed by comparative 2−ΔΔCt method.

The relative gene expression was analysed by comparative 2−ΔΔct method.

Transgene expression was analysed by western blotting with 2 μg anti-c-MYC (Sigma, C3956) antibody or HERK1 antibody as control.

Integrin expression was analysed by qPCR, which showed the extent of spatial and temporal regulation achieved by the nanopores.

Dll4 expression was analysed by RQ-PCR and flowcytometry.