The SLC6A4 promoter VNTR polymorphism was genotyped
by agarose gel size fractionation as described in ref.
The resulting PCR products were separated
by agarose gel electrophoresis.
Digested DNA was visualized
by agarose gel (1.5 — 2.0 %).
Ten - microliter aliquots of the nested PCR products were subjected to RFLP analysis by digestion with 2 U of either HinfI or MseI, and digested fragments were resolved
by agarose gel electrophoresis in TBE buffer, as described elsewhere [19, 28].
The resulting DNA fragments are analyzed
by agarose gel electrophoresis.
Not exact matches
Amplified sequences were visualized
by gel electrophoresis in 2 %
agarose gels stained with GelRed (Biotium).
PCR products were separated
by electrophoresis on a 2 %
agarose gel, stained with ethidium bromide and visualized
by UV illumination.
PCR products were visualized
by electrophoresis in an ethidium bromide - stained 1.8 %
agarose gel.
After a traditional PCR has been completed, the data are analyzed
by resolution through an
agarose gel or, more recently, through a capillary electrophoresis system.
DNA libraries were then re-amplified for another 13 cycles in quintuplicates or sextuplicates, followed
by pooling and purification, visual inspection on a 3.5 %
agarose gel, and final quantification using a NanoDrop 2000c spectrophotometer (FisherScientific).
PCR products were separated
by gel electrophoresis on 2 %
agarose gel.
The resulting PCR amplification products were analyzed
by electrophoresis in 1.5 %
agarose gels.
At 24 hours post fertilization (hpf), fluorescent embryos were dechorionated, mounted on coverslips in 1.2 % ultra-low
gelling agarose, overlaid with 30 % Danieua / PTU and analyzed
by laser scanning confocal microscopy (Zeiss LSM510 Meta).
PCR products were visualized
by blue light after electrophoresis on a 2.5 %
agarose gel containing 1 × GelStar ® Nucleic Acid Gel Stain (Lonza, Breda, The Netherlands) in 1 × Tris - borate buffer (pH 8.
gel containing 1 × GelStar ® Nucleic Acid
Gel Stain (Lonza, Breda, The Netherlands) in 1 × Tris - borate buffer (pH 8.
Gel Stain (Lonza, Breda, The Netherlands) in 1 × Tris - borate buffer (pH 8.0).