Determination of nuclear transcription factor activity using a modified electrophoretic mobility shift assay

Abstract

In this work, several major procedures of the electrophoretic mobility shift assay (EMSA) were modified including swift extraction of the nucleic protein, labeling of the probe and radioautography. The modified assay required shorter time, simplified the nucleic protein extraction, increased the radioactivity of the labeling probe, skipped the tedious process of gel drying, and produced clear images. Its results were comparable, reproducible and stable. It thus has merited for wide application.<br>A determinação da alteração na mobilidade eletroforética (EMSA), o método de mais ampla utilização para o estudo das interações proteínaácidos nucléicos, é tediosa e difícil de dominar. De acordo com os protocolos dacumentados e com base em nossa prática, nós modificamos os diversos processos principais dessa determinação incluindo no que diz respeito a extração de proteiínas nucleicas, marcação das provas e radioautografia. A determinação modificada requer menor tempo, simplifica a extração de ácidos nucleicos, eleva a radioatividade da prova marcada, evita o processo tedioso de secagem do gel e produz claras imagens. Seus resultados são comparáveis, reproduzíveis e estáveis, merecendo, desse modo, ampla aplicação

Inhibitory Effect of Curcumol on Jak2-STAT Signal Pathway Molecules of Fibroblast-Like Synoviocytes in Patients with Rheumatoid Arthritis

“…A chemiluminescent detection method utilizing a luminol/enhancer solution and a stable peroxide solution (Pierce, USA) was used as described by the manufacturer, and membranes were exposed to X-ray films for 2 min before developing. The bands were scanned, and relative intensities were analyzed by Labwork Analysis Software [ 18 , 19 ].…”