Sentence examples for the samples were electrophoresed using from inspiring English sources

The samples were electrophoresed using Tricine-SDS gels to reveal any resulting cleavage products (Figure 6A).

The samples were electrophoresed using 2% agarose gels.

Samples were electrophoresed using the NuPAGE system (Invitrogen), transferred onto PVDF (Millipore) membranes and blocked as described previously (Haigh et al., 2009) with the exception of PrP blots, which used 2% (w/v) ECL Advance buffer with ECL Advance developer (GE Healthcare, Sydney, NSW, Australia).

Protein samples were electrophoresed using Bis-Tris NuPage gels (Invitrogen) and transferred using the iBlot dry blotting system (Invitrogen).

RNA samples were electrophoresed using denaturing (formamide/ formaldehyde) agarose gels to qualitatively assess for any degradation that may have occurred during the isolation.

Samples were electrophoresed using 10% sodium dodecyl sulfate-polyacrylamide gels under reducing conditions and electrotransferred onto polyvinylidene fluoride (PVDF) membrane (Immobilon® FL, Millipore) or nitrocellulose (Bio-Rad).

In total, 50  μg of each sample was electrophoresed using a sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto Hybond nitrocellulose membranes (Amersham, USA).

The protein samples (10 15 µg) were electrophoresed using a 10 12% SDS-polyacrylamide electrophoresis gel.

After cooling, each sample was loaded in three portions into separate lanes on an SDS PAGE gel and the proteins were electrophoresed using a 4 12% Bis-Tris gel with MES as the running buffer.

The worm lysates were electrophoresed using 8% SDS‐PAGE and transferred to PVDF membrane.

Samples (~40 μg per lane) of the midgut protein extract were electrophoresed using NuPage 4 – 12% 1 mm thick gradient gels under reducing conditions in accordance with the manufacturer's instructions (Invitrogen).