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LD statistics were calculated and haplotype blocks were visualized by using the Haploview software [42].
Synteny blocks were visualized by using Circos26.
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The blots were visualized by ECL GE HealthcareECL GE Healthcare
Segmental blocks were visualized using the software Circos-0.55 [ 48].
After blocking and appropriate incubation with primary and secondary antibodies, protein signals were visualized by enhanced chemiluminescence (Thermo Scientific, Rockford, IL, USA).
pSmad1/5 and pErk1/2 were visualized by incubation the given antibodies diluted at 1 200 in blocking solution [PBT+10% normal goat serum (NGS)] overnight at 4°C.
Both particles were visualized by TEM.
Polymer remnants were visualized by polarization microscopy.
Cell nuclei were visualized by DAPI staining.
Nanoparticles were visualized by negative staining microscopy.
Protein bands were visualized by ECL.
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