Oct 11, 2022

Public workspaceADN PURIFICATION FROM AGAROSE GELS WITH GENELUTE GEL EXTRACTION KIT

DOI
dx.doi.org/10.17504/protocols.io.kxygx9p5dg8j/v1
  • 1Tecnologico de Monterrey Campus Chihuahua
Georgina Elisa Diego Macías
Icon indicating open access to content
QR code linking to this content
DOI: dx.doi.org/10.17504/protocols.io.kxygx9p5dg8j/v1
Protocol Citation: Ana Belem García González, Georgina Elisa Diego Macías, Irán Alessandra Chaparro Rodríguez, Jair Alexis Gardea Sáenz 2022. ADN PURIFICATION FROM AGAROSE GELS WITH GENELUTE GEL EXTRACTION KIT . protocols.io https://dx.doi.org/10.17504/protocols.io.kxygx9p5dg8j/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: October 11, 2022
Last Modified: October 11, 2022
Protocol Integer ID: 71132
Abstract
Protocol for DNA purification from DNA purification from agarose gels with GeneElute Gel Extraction Kit
Materials
GenElute Gel Extraction Kit (NA1111, Sigma-Aldrich):
  • Column Preparation Solution
  • Gel Solubilization Solution
  • Wash Solution Concentrate G
  • Elution Solution
  • GenElute Binding Column G
  • Collection Tubes, 2 mL
Isopropanol
Ethanol
Sodium Acetate 3M, pH 5.2
Thermoblock at 50-60°C.
Electrophoresis equipment for agarose gel
Tubes of 1.5 mL

Previous electrophoresis : Realization of an electrophoresis in a agarose gel of the product of ADN, charging the maximum amount of DNA per well (if necessary, use more than one well)
Extraction of the band of interest: Extract the band of interest of the gel, removing the excess of agarose
Weighting the band: Weight the piece of gel removed in a tarated tube.
Gel Solubilization: Add 3 volumes of Gel Solubilization Solution to the piece of gel, meaning, for each Amount100 mg of agarose gel, add Amount300 µL of Gel Solubilization Solution. Incubate at 50-60°C for Duration00:10:00 minutes or until the piece of gel has completely dissolved. Give Vortex every 2 or 3 minutes in this incubation time.

10m
Preparation of the column (This can be done alongside step 4). Add GenElute Binding Column G in a recolectation tube of 2 mL. Add Amount500 µL of the Column Preparation Solution to each Binding Column. Centrifugate for Duration00:01:00 minute at 12,000 to 16,000 x g. Discard liquid

1m
Check the color of the sample: Once the gel had dissolved completely, make sure that the color is yellow before continuing. If the color is red, add Amount10 µL of the Sodium Acetate 3M, pH 5.2 buffer and mix. Add until the color is yellow.

Add isopropanol: Add a volume of the gel of isopropanol at 100% and mix until homogenized.
Bind ADN: Charge the sample of step 7 to the binding column prepared in step 5. Is normal a change of color from yellow to red once the sample is charged. If the volume of the sample is bigger than Amount700 µL , charge the sample in proportions of Amount700 µL . Centrifugate for one minute at 12,000-16,000 x g every time after the sample is charged. Discard the liquid obtained from the centrifugation.

Wash the column: Add Amount700 µL of Wash Solution to the binding column. Centrifugate for one minute at 12,000-16,000 x g. Remove the binding column of the tube and discard liquid. Colocate again the binding column in the recollection tube and centrifuge one more time for one minute to eliminate the excess of ethanol

Elute the DNA: Transfer the binding column to a clean, esteril tube. Add Amount50 µL of the Elution Solution to the center of the membrane and incubate forDuration00:01:00 minute. Centrifuge for Duration00:01:00 minute at 12,000-16,000 x g. In case of purifying plasmid DNA or linear fragmented of DNA with a weight exceeding 3Kb, preheat the Elute Solution at 65 °C

2m