Nzygelpure: Catalogue Number: Mb01101, 50 Columns

NZYGelpure
Catalogue number: MB01101, 50 columns

MB01104, 2 x 50 columns
MB01102, 200 columns
MB01103, 5 x 200 columns
Description
NZYGelpure kit is designed for the purification of DNA from TAE/TBE agarose gels and
for the direct purification of PCR products. The kit can be used to purify DNA fragments
from 50 bp to 20 kb. Average recoveries range from 60 to 90% depending on the
fragment size. NZYGelpure purification kit utilizes a silica-gel based membrane which
selectively adsorbs up to 20 µg of DNA fragments in the presence of specialized
binding buffers. Soluble agarose, nucleotides, oligos (<30-mer), primer dimers,
enzymes, mineral oil and other impurities do not bind to the membrane and are
washed away. DNA fragments are then eluted off the column and can be used for
downstream protocols without further processing. Binding Buffer contains a pH
indicator, allowing the evaluation of optimal pH for DNA binding. The pH indicator does
not interfere with DNA binding.
Storage conditions and reagents preparation

All kit components can be stored at room temperature (20-25 °C) and are stable till the
expiry date. Add 48 mL (MB01101) or 2  100 mL (MB01102) of ethanol to each bottle
of Wash Buffer.
System Components
Component 50 columns 200 columns
Binding Buffer 2  30 mL 2  120 mL

Wash Buffer (concentrate) 12 mL 2  25 mL
Elution Buffer (does not contain EDTA) 15 mL 60 mL
NZYTech Spin Columns 50 200
Collection Tubes (2 mL) 50 200
Protocol for plasmid DNA purification from Agarose Gels
All purification steps should be carried out at room temperature.
All centrifugations should be carried out at room temperature in a table-top

microcentrifuge at >12000 xg (10000-15000 rpm depending on the rotor type).
1. Excise the DNA fragment from the gel with a clean, sharp scalpel. Weight the gel
slice and transfer to a 1.5 mL microcentrifuge tube.
2. Add 300 µL of Binding Buffer for each 100 mg of gel weight (example – a gel slice
weighing 125 mg would require 375 µL of Binding Buffer). For high concentration gels
(2.0-3.0%), 500 µL of Binding Buffer per 100 mg of agarose gel should be added. The
maximum amount of gel slice per NZYTech spin column is 400 mg. For gel slices >400
mg use more than one column.
3. Incubate at 55-60 °C for 5-10 minutes and shake occasionally until agarose is
completely dissolved.
4. Check that the colour of the mixture is yellow (similar to the colour of the Binding
Buffer). If the colour of the mixture is orange or violet, add 10 µL of 3 M sodium acetate
pH 5.0, and mix well.
5. (Optional) For DNA fragments <500 bp or >10 kb long add 1 gel volume of
isopropanol to the sample and mix well by pipetting several times (example – a gel slice
weighing 125 mg would require 125 µL of isopropanol).
6. Load the above mixture into the NZYTech spin column placed into a Collection tube
(2 mL). Centrifuge for 30s to 1 minute and discard the flow-through in the collection
tube. The maximum volume of the column reservoir is 700 µL. For sample volumes of
more than 700 µL, simply load and spin again.
7. (Optional) Add 500 µL of Wash Buffer and centrifuge for 30s to 1 minute. Discard
the flow-through in the collection tube. This step is only important if DNA is intended
to be used for direct sequencing, in vitro transcription or microinjection.
8. Add 600 µL of Wash Buffer and centrifuge for 30s to 1 minute. Discard the flow-
through in the collection tube.
9. Centrifuge for 1 minute to dry NZYTech spin membrane of residual ethanol.
10. Place the NZYTech spin column into a clean 1.5 mL microcentrifuge tube. Add 50 µL
of Elution Buffer to the centre of the column and incubate at room temperature for 1
minute. Centrifuge for 1 minute to elute DNA. Ultrapure water (pH 7.5-8.5) may be used
in place of elution buffer. However, DNA recovery with acidic waters may be
significantly reduced.
11. Store the purified DNA at -20 °C.

Notes (elution step):
1. It is extremely important to add the Elution Buffer to the centre of the column.
Incubating the column at higher temperatures (37 to 50 °C) may slightly increase the
yield. Pre-warming the Elution Buffer at 55 to 80 °C may also slightly increase elution
efficiency.
2. If a higher DNA concentration is desirable, 30 µL (or less) of Elution Buffer can be
used to elute the DNA. It is critical that the Elution Buffer is applied directly in the
centre of the column. (To recover maximum amount of DNA it is recommended to
repeat the elution step.)
3. If water is used for elution, make sure that its pH is between 7.5 and 8.5. Elution
efficiency is dependent on pH and the maximum elution efficiency is achieved within
this range. A pH <7.0 can decrease yield.
Protocol for PCR clean-up or DNA purification from enzymatic reactions

All purification steps should be carried out at room temperature.
All centrifugations should be carried out at room temperature in a table-top

microcentrifuge at >12000 xg (10000-15000 rpm depending on the rotor type).
1. Transfer the volume of the reaction mixture into a 1.5 mL microcentrifuge tube and
add five volumes of Binding Buffer. Mix by inverting the tube a few times. Centrifuge
briefly to collect the sample. All purification steps including centrifugation should be
carried out at room temperature.
Notes (sequencing of PCR products):
When cleaning up PCR products for subsequent sequencing processes, if using an

amplification primer for sequencing avoid primers larger than 22-25 bp. In this case it is
recommended to use a maximum of 0.25 µM of primers during the PCR amplification
and 2.5 µM of the sequencing primer in the sequencing reaction. In case residual peaks
appear in sequencing chromatograms, due to the presence of traces of the second
amplification primer, dilute Binding Buffer to a 60-50% solution in water and proceed as
above. Use NZYTech sequencing services for maximum efficiencies.
2. Add the above mixture to the NZYTech spin column. The maximum loading volume
of the column is 700 µL. For sample volumes greater than 700 µL simply load again.
Centrifuge for 30s to 1 minute and discard the flow-through in the tube.
3. Add 600 µL of Wash Buffer and centrifuge for 30s to 1 minute. Discard the flow-
through in the collection tube.
4. Centrifuge for 1 minute to dry NZYTech spin membrane of residual ethanol.

5. Place the NZYTech spin column into a clean 1.5 mL microcentrifuge tube. Add 50 µL
of Elution Buffer to the centre of the column and incubate at room temperature for 1
minute. Centrifuge for 1 minute to elute DNA. Ultrapure water may be used in place of
elution buffer. However, DNA recovery with acidic waters may be significantly reduced.
(Please check elution notes in previous section).
6. Store the purified DNA at -20 °C.
Quality control assay

All components of NZYGelpure kit are tested following the isolation protocol described
above for the purification of DNA fragments from agarose gels and PCR reactions.
Revised 07/17
Certificate of Analysis
Test Result
Functional assay Pass
Approved by:
José Prates
Senior Manager, Quality Systems
Estrada do Paço do Lumiar,

Campus do Lumiar - Edifício E, R/C
1649-038 Lisboa, Portugal
Tel.:+351.213643514
Fax: +351.217151168
www.nzytech.com

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NZYGelpure

Catalogue number: MB01101, 50 columns

Storage conditions and reagents preparation

Component 50 columns 200 columns

Binding Buffer 2  30 mL 2  120 mL

All centrifugations should be carried out at room temperature in a table-top

9. Centrifuge for 1 minute to dry NZYTech spin membrane of residual ethanol.

11. Store the purified DNA at -20 °C.

Protocol for PCR clean-up or DNA purification from enzymatic reactions

All centrifugations should be carried out at room temperature in a table-top

Notes (sequencing of PCR products):

When cleaning up PCR products for subsequent sequencing processes, if using an

4. Centrifuge for 1 minute to dry NZYTech spin membrane of residual ethanol.

6. Store the purified DNA at -20 °C.

Quality control assay

Functional assay Pass

Estrada do Paço do Lumiar,

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