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Bound proteins were resolved by PAGE, transferred onto PVDF membranes, and analyzed by immunoblotting.

Crude protein extracts were run in 15% PAGE, transferred to a nitrocellulose membrane and stained with Coomassie Blue.

Boiled samples with sample buffer were separated on 8 15% SDS polyacrylamide gel electrophoresis (PAGE), transferred to nitrocellulose membrane.

These were separated by SDS polyacrylamide gel electrophoresis (PAGE), transferred to PVDF membrane, and analyzed by immunoblotting.

Proteins were resolved by 8%122% SDS-PAGE, transferred to nitrocellulose membranes, and probed with primary and secondary antibodies.

Biotinylated samples were run on SDS-PAGE, transferred to a nylon membrane, and detected with nucleic acid detection kit (Thermo).

Biotinylated samples were run on SDS-PAGE, transferred to a nylon membrane (400 mA for 1.5 h), and detected with nucleic acid detection kit (Thermo).

Immunoprecipitates were subjected to SDS-PAGE transferred to PVDF membrane.

Immunoprecipitated proteins were separated by SDS-PAGE, transferred to nitrocellulose, and detected by Western Blot analysis.

Equal amounts of protein were loaded on a 12% SDS-PAGE, transferred to nitrocellulose membrane.

Complexes were separated by SDS-PAGE, transferred to PVDF and blocked in 5% milk overnight.