Responsible and highly motivated professional with solid and diverse experience as Molecular Biologist with excellence in isolating and purifying DNA, bacterial plating, polyacrylamide gel electrophoresis,
agarose gel electrophoresis.
Analytical tools: Thin layer chromatography, UV / Visible spectrophotometry, microcentrifuge, metabolism chamber, compound microscope, dissecting microscope, SDS - PAGE, PCR,
agarose gel electrophoresis.
This activity introduces DNA analysis through DNA digestion with restriction enzymes and
agarose gel electrophoresis.
The resulting PCR products were separated by
agarose gel electrophoresis.
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 improved size resolution of the DNA chip allows students to identify their genotype, something impossible with
agarose gel electrophoresis.
The resulting DNA fragments are analyzed by
agarose gel electrophoresis.
Not exact matches
Runtimes are approximately one hour versus up to 16 hours needed for methods such as
agarose - based, pulsed - field
gel electrophoresis.
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.
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.
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).
Performed various tasks in the lab such as preparing
agarose gels and buffer dilutions for
electrophoresis.