Exact(2)
Cell fractionation was performed using the nuclear extract kit according to the manufacturer's instruction (Active Motif, Carisbad, CA, USA).
The nuclear and cytoplasmic extracts from bone marrow-derived macrophages were prepared, as per the manufacturer's instruction (Active Motif, Carlsbad, CA, USA).
Similar(58)
RUNX-2 and PPARγ transcription factor activity was determined using a commercial TransAM™ assay as per manufacturers instructions (Active Motif, Belgium).
Antibody supershift reactions were performed following manufacturers instructions (Active Motif, Carlsbad, CA).
Nuclear extracts was prepared with a Nuclear Extract Kit according to manufacturer instructions (Active Motif, Carlsbad, CA).
To quantify active Runx2 binding, 15 20 mg of nuclear extract was measured using the Trans-AM Runx2 Kit according to the manufacturer's instructions (Active Motif, Carlsbad, CA, USA).
Nuclear extracts from the cells were prepared and p65 DNA binding activity was measured using the TransAM™ NFκB kit according to the manufacturer's instructions (Active Motif, Carlsbad, CA).
ChIP assays were performed according to the manufacturer's instructions (Active Motif, USA).
Nuclear extracts were prepared from C2C12/Runx2Dox cells treated with Dox according the manufacturer's instructions (Active Motif, Carlsbad, CA, USA).
NF-κB activation was assessed using the TransAM NF-κB kit according to the manufacturer's instructions (Active Motif, Belgium).
Nuclear extracts were prepared using a nuclear isolation kit and according to the manufacturer's instructions (Active Motif).
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