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MilliporeSigma

NA1020

GenElute PCR Clean-Up Kit

sufficient for 70 purifications

GenElute™ PCR Clean-Up Kit

Synonym(s):

Gen Elute, PCR Purification

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1 KIT

$197.00

$197.00


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About This Item

UNSPSC Code:
41106300
NACRES:
NA.52

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usage

sufficient for 70 purifications

technique(s)

DNA purification: suitable

storage temp.

15-25°C

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This Item
NA1111NA9604G1N10
usage

sufficient for 70 purifications

usage

sufficient for 70 purifications

usage

sufficient for 4 96-well plate purifications

usage

sufficient for 10 purifications

technique(s)

DNA purification: suitable

technique(s)

DNA purification: suitable

technique(s)

DNA purification: suitable

technique(s)

-

PCR9601

-

NA0150, NA0150S, NA0160

G1N350, G1N70, G1N9602, G1N9604

storage temp.

15-25°C

storage temp.

15-25°C

storage temp.

15-25°C

storage temp.

15-25°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

General description

The GenElute PCR Clean-Up Kit is designed for rapid purification of single-stranded or double-stranded PCR amplification products (100 bp to 10 kb) from other components in the reaction, such as excess primers, nucleotides, DNA polymerase, oil and salts. This kit combines the advantages of silica binding with a convenient spin column format, eliminating the need for expensive resins or toxic organic compounds such as phenol and chloroform.

DNA is bound on a silica membrane within the spin column. The bound DNA is washed and the clean, concentrated DNA is eluted in the buffer of choice. Each column can purify up to 100 μL or 10 μg of PCR amplified DNA and recover up to 95% of PCR products between 100 bp and 10 kb. More than 99% of the primers and most primer-dimers (<40 bp) are removed.

Purified DNA can be used in enzymatic reactions, conventional or automated sequencing, cloning and microarray analysis.

Application

GenElute PCR Clean-Up Kit has been used for rapid purification of single-stranded or double-stranded PCR amplification products (100bp to 10kb) from other components in the reaction.[1][2][3]
Purified DNA can be used in enzymatic reactions, conventional or automated sequencing, cloning and microarray analysis.

Biochem/physiol Actions

The GenElute PCR Clean-Up Kit combines the advantages of silica binding with a microspin format. The DNA is bound on a silica membrane within the spin column. The bound DNA is washed and the clean, concentrated DNA is eluted in the buffer of choice. Each column can purify up to 100 μL or 10 μg of PCR amplified DNA and recover up to 95% of PCR products between 100 bp and 10 kb. More than 99% of the primers and most primer-dimers (<40 bp are removed).

Features and Benefits

  • Purifies up to 100 μl or 10 μg of PCR amplified DNA in 8 minutes
  • Recovers up to 95% of PCR products between 100 bp and 10 kb
  • Removes over 99% of primers and other components
  • Eliminates the need to remove mineral oil by organic extraction
  • 40% more purification preps supplied than market leader
  • Recovers up to 95% of PCR products between 100 bp and 10 kb
  • Purifies up to 100 μL or 10 μg of PCR amplified DNA in 8 minutes
  • Removes over 99% of primers and other components

Other Notes

The GenElute PCR Clean-Up Kit is designed for rapid purification of single-stranded or double-stranded PCR amplification products (100 bp to 10 kb) from other components in the reactions, such as excess primers, nucleotides, DNA polymerase, oil and salts. This kit combines the advantages of silica binding with a convenient spin column format, eliminating the need for expensive resins or toxic organic compounds such as phenol and chloroform.

Legal Information

GenElute is a trademark of Sigma-Aldrich Co. LLC

Kit Components Also Available Separately

Product No.
Description
SDS

  • C2112Column Preparation SolutionSDS

pictograms

CorrosionExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

8A - Combustible corrosive hazardous materials

flash_point_f

Not applicable

flash_point_c

Not applicable


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Andreas Veith et al.
Frontiers in microbiology, 2, 37-37 (2011-07-13)
The sulfur oxygenase reductase (SOR) is the initial enzyme of the sulfur oxidation pathway in the thermoacidophilic Archaeon Acidianus ambivalens. The SOR catalyzes an oxygen-dependent sulfur disproportionation to H(2)S, sulfite and thiosulfate. The spherical, hollow, cytoplasmic enzyme is composed of
Isolation of disseminated neuroblastoma cells from bone marrow aspirates for pretreatment risk assessment by array comparative genomic hybridization.
Vandewoestyne M
International Journal of Cancer. Journal International Du Cancer, 130(5), 1098-1108 (2012)
Kathleen Gärtner et al.
Retrovirology, 6, 32-32 (2009-04-08)
Foamy viruses (FVs) are the most genetically stable viruses of the retrovirus family. This is in contrast to the in vitro error rate found for recombinant FV reverse transcriptase (RT). To investigate the accuracy of FV genome copying in vivo
Elisabeth Ullrich et al.
Journal of biotechnology, 310, 80-88 (2020-02-06)
We have identified 24 molecular markers, based on circulating nucleic acids (CNA) originating from the human genome, which in combination can be used in a quantitative real-time PCR (qPCR) assay to identify the presence of human sepsis, starting two to
Charlotte G Cole et al.
Genome biology, 9(5), R78-R78 (2008-05-15)
Although the human genome sequence was declared complete in 2004, the sequence was interrupted by 341 gaps of which 308 lay in an estimated approximately 28 Mb of euchromatin. While these gaps constitute only approximately 1% of the sequence, knowledge

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Overview of common techniques and downstream applications for extraction and purification of genomic DNA, plasmid DNA, and total RNA from cells, tissue, blood, viruses, and other sample types.

Questions

1–8 of 8 Questions  
  1. What is the elution buffer made of? As it can be replaced with water, is it just water that is provided?

    1 answer
    1. The specific composition of the elution buffer E7777 is considered proprietary. However it is a Tris-HCL solution without EDTA.

      Helpful?

  2. Does this kit remove proteins from PCR product?

    1 answer
    1. This is a post-pcr clean up kit. The single or double-stranded amplification products are bound to the silica membrane. Then all non-DNA material such as primers, nucleotides, and polymerase are washed away. Finally the purified product is eluted. Anything that isn't bound will be removed.

      Helpful?

  3. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

      Helpful?

  4. Can Product NA1020, GenElute™ PCR Clean-Up Kit, be used for isolation of PCR products labeled with digoxigenin?

    1 answer
    1. Although we have not tested the kit with digoxigenin-labeled PCR products specifically, it should be fine to use

      Helpful?

  5. Can Product No. NA1020, GenElute™ PCR Clean-Up Kit,  be used to clean up PCR products larger than 10 kb?

    1 answer
    1. We haven't tested anything bigger than 10 kb, but we would expect larger DNA to bind well.  That said, the bound DNA might be more difficult to elute.  Heating the elution solution to 60-65°C may help with elution.  Incubating a few minutes to allow the elution solution to soak into the binding matrix may also help.

      Helpful?

  6. When using Product No. NA1020, GenElute™ PCR Clean-Up Kit, what is the largest amount of PCR reaction sample that can be processed on one column?

    1 answer
    1. The upper limit on the PCR reaction volume that can be cleaned up is 100 μl. In that scenario, 500 μl of binding solution would be added for a total of 600 μl volume being applied to the column.

      Helpful?

  7. When using GenElute™ PCR Clean-Up Kit, Product No. NA1020, Can the amount of elution buffer be reduced in order to obtain a more concentrated eluate?

    1 answer
    1. One may indeed increase concentration by reducing elution volume, but we would not suggest going lower than 25-30 μl. One must keep in mind that if a volume of less than 50 μl is used (for example, 30 μl), the concentration will increase, but the total yield will also be reduced.

      Helpful?

  8. Can GenElute™ PCR Clean-Up Kit, Product NA1020, be used for isolation of labeled PCR products?

    1 answer
    1. This kit will work with labeled PCR products and no modifications to the standard protocol are needed.

      Helpful?

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