This is 1 million times more sensitive than the typical concentration for an analysis
on agarose gel.
Not exact matches
Conditions for the PCR reaction were 40 cycles of 94 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s. Amplicons were purified
on a 2 %
agarose gel, cloned into plasmid vectors using TOPO TA (Invitrogen, Carlsbad, CA), and sent to an outside company (Elim Biopharmaceuticals, Hayward, CA) for Sanger sequencing in both directions using vector primers M13F and M13R.
PCR products were separated by electrophoresis
on a 2 %
agarose gel, stained with ethidium bromide and visualized by UV illumination.
The amplified DNA products were analyzed
on a 1.0 %
agarose gel, and pieces of
gel containing the amplified DNA bands were excised and purified using a
gel extraction kit (Takara Bio).
c, Southern blot (left) membrane hybridization of 10 µg of BamHI - digested genomic DNA (see corresponding
agarose gel on right) using a DNA probe from the pCEP backbone.
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.
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).
Products were resolved
on a 2 %
agarose gel.