Pembuatan DNA Ladder 100 bp Berbasis Polymerase Chain Reaction secara Mandiri
Abstract
Introduction. Polymerase chain reaction (PCR) is a rapid progress in molecular biology
and is widely used in diagnosing diseases and genetic engineering. The PCR results
interpretation needs an electrophoresis approach which requires a DNA ladder as an
indicator of DNA size. Currently, Indonesia relies on commercial DNA ladders from
abroad. Imported DNA ladder takes cost and transportation time. Therefore, Indonesia
needs to produce DNA ladders. Objective. This study aims to produce homemade 100 bp
DNA ladder. Methods. DNA from blood was isolated using the isolation kit (GIN-170,
Sgima-Aldrich). Primer sets for 100, 200, 300, 400, 500, 600, 700, 800, 900, and 1000 bp
were designed using Primer-BLAST. The expected DNA bands were produced by routine
PCR and visualized using 2% (w/v) agarose gel electrophoresis. Amplicons were mixed to
be a 100 bp DNA ladder. The homemade 100 bp DNA ladder was compared to the
commercial one. Results and Discussion. The isolated DNA purity reached 1.878. Routine
PCR produces bands of 100, 200, 300, 400, 500, 600, 700, 800, 900, and 1000 bp. The
concentration of band 100, 500 and 1000 were 300 ng and the others were 200 ng. Mixing
each band produces a 100 bp DNA ladder. Conclusion. A homemade 100 bp DNA ladder
were produced using human blood DNA and has as good quality as a commercial one.
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