Catalog #	Size	List Price	Your Price
T1030L	250 preps
T1030S	50 preps	$152.00	$136.80

The Monarch PCR & DNA Cleanup Kit rapidly and reliably purifies up to 5 μg of concentrated, high-quality DNA from PCR and other enzymatic reactions. The kit utilizes a bind/wash/elute workflow with minimal incubation and spin times. The columns ensure zero buffer retention and no carryover of contaminants, enabling elution of sample in volumes as low as 6 μl. The buffers provided have been optimized, and do not require monitoring of pH. Eluted DNA is ready for use in restriction digests, DNA sequencing, ligation and other enzymatic manipulations. Designed with sustainability in mind, Monarch kits use significantly less plastic and responsibly-sourced, recyclable packaging. The protocol can also be modified to enable the purification of smaller DNA fragments, including oligonucleotides and ssDNA.

View our videos on protocols, tips, and recycling Monarch.

APPLICATIONS
PCR cleanup	DNA from PCR reactions can be purified after amplification to remove polymerases, primers, detergents, dNTPs, etc.
Enzymatic reaction cleanup	Restriction enzymes and modifying enzymes such as ligases, kinases, nucleases, phosphatases are efficiently removed, allowing for effective desalting and concentration of the DNA sample.
cDNA cleanup	DNA/RNA complexes can be purified post-reverse transcription/amplification to enable removal of the RT and polymerase as well as nucleotides.
Labeling cleanup	Unincorporated radiolabeled or fluorescently labeled nucleotides can be removed from the DNA substrate
Plasmid cleanup	Plasmid preps from unknown sources may contain inhibitors and unwanted contaminants. Purification and concentration can be easily achieved using this kit.
Oligonucleotide cleanup	ssDNA oligonucleotides (≥ 18 nt) and dsDNA fragments (≥ 15 bp) can be purified using the Oligonucleotide Cleanup Protocol.

Monarch columns are designed for performance. Monarch columns are designed without a frit, which eliminates buffer retention and the risk of carryover contamination, providing fast, worry-free DNA purification. — Monarch columns are designed without a frit, which eliminates buffer retention and the risk of carryover contamination, providing fast, worry-free DNA purification.

Specifications

DNA Sample Type:	DNA from PCR and other enzymatic reactions (e.g., restriction digests, kinase reactions, ligations). ssDNA or dsDNA oligonucleotides from enzymatic reactions can also be purified using the Oligonucleotide Cleanup Protocol.
Binding Capacity:	up to 5 μg
DNA Size Range:	~50 bp to 25 kb DNA ≥ 15 bp to 25 kb (dsDNA) and DNA ≥ 18 nt to 10 kb (ssDNA) can also be purified using the Oligonucleotide Cleanup Protocol.
Typical Recovery:	DNA (50 bp to 10 kb): 70–90% DNA (11–23 kb): 50–70% ssDNA ≥ 18 nt and dsDNA ≥ 15 bp: 70-85%
Elution Volume:	≥ 6 μl
Purity:	A_260/280 > 1.8 and A_260/230 > 1.8
Protocol Time:	5 minutes of spin and incubation time
Compatible Downstream Applications:	ligation, restriction digestion, labeling and other enzymatic manipulations, library construction and DNA sequencing.

Monarch PCR & DNA Cleanup Kit (5 µg) Protocol

Monarch PCR & DNA Cleanup Kit (5 μg) performs equivalently to the leading supplier. Preps were performed according to recommended protocols. 1 μg of a 3 kb DNA fragment was incubated with 1 μM primers and OneTaq® Quick-Load® 2X Master Mix (NEB #M0486). DNA was eluted in 20 μl (NEB) and 40 μl (Qiagen) Elution Buffer. Half of the total elution volume was digested with 5 units of DraIII-HF® (NEB #R3510). The digest and the unused portion of the elution were resolved on a 1% w/v agarose gel along with a representative sample of the starting material. — Preps were performed according to recommended protocols. 1 μg of a 3 kb DNA fragment was incubated with 1 μM primers and OneTaq® Quick-Load® 2X Master Mix (NEB #M0486). DNA was eluted in 20 μl (NEB) and 40 μl (Qiagen) Elution Buffer. Half of the total elution volume was digested with 5 units of DraIII-HF® (NEB #R3510). The digest and the unused portion of the elution were resolved on a 1% w/v agarose gel along with a representative sample of the starting material.

Monarch PCR & DNA Cleanup Kit (5 μg) removes low molecular weight primers from dsDNA samples. Three independent amplicons (267 bp, 520 bp, 1003 bp) were spiked with two oligonucleotides (16-mer, 24-mer) to a final concentration of 1 μM. Half of each mix was purified with the Monarch PCR & DNA Cleanup Kit (5 μg) following the included protocol. Equivalent fractions of the original mixture and the eluted material were resolved on a 20% TBE acrylamide gel at 100V for one hour and stained with SYBR Green II. — Three independent amplicons (267 bp, 520 bp, 1003 bp) were spiked with two oligonucleotides (16-mer, 24-mer) to a final concentration of 1 μM. Half of each mix was purified with the Monarch PCR & DNA Cleanup Kit (5 μg) following the included protocol. Equivalent fractions of the original mixture and the eluted material were resolved on a 20% TBE acrylamide gel at 100V for one hour and stained with SYBR Green II.

Features

Elute in as little as 6 μl
Prevent buffer retention and salt carry-over with optimized column design
Save time with fast, user-friendly protocols
No need to monitor pH
Buffers and columns available separately
Responsibly-sourced and recyclable packaging
Significantly less plastic used when compared with other kits

MonarchÂ® PCR & DNA Cleanup Kit (5 Î¼g) | Purification Kits | New England Biolabs

Home Discontinued Monarch^® PCR & DNA Cleanup Kit (5 μg)

Monarch^® PCR & DNA Cleanup Kit (5 μg)

Replaced by Monarch^® Spin PCR and DNA Cleanup Kit (5 μg) on December 02, 2024

Catalog # T1030 was discontinued on December 02, 2024

Quickly and easily purify high quality DNA from PCR and other enzymatic reactions.

Elute in as little as 6 μl
Prevent buffer retention and salt carry-over with optimized column design
Save time with fast, user-friendly protocols
No need to monitor pH
Protocol modification allows for ssDNA purification, oligonucleotide purification, and purification of other small DNA fragments
Buffers and columns available separately
Significantly less plastic used when compared with other kits
Responsibly-sourced and recyclable packaging

Check out our Technical Note containing comprehensive insights into measuring and analyzing nucleic acids.

Product Information

APPLICATIONS
PCR cleanup	DNA from PCR reactions can be purified after amplification to remove polymerases, primers, detergents, dNTPs, etc.
Enzymatic reaction cleanup	Restriction enzymes and modifying enzymes such as ligases, kinases, nucleases, phosphatases are efficiently removed, allowing for effective desalting and concentration of the DNA sample.
cDNA cleanup	DNA/RNA complexes can be purified post-reverse transcription/amplification to enable removal of the RT and polymerase as well as nucleotides.
Labeling cleanup	Unincorporated radiolabeled or fluorescently labeled nucleotides can be removed from the DNA substrate
Plasmid cleanup	Plasmid preps from unknown sources may contain inhibitors and unwanted contaminants. Purification and concentration can be easily achieved using this kit.
Oligonucleotide cleanup	ssDNA oligonucleotides (≥ 18 nt) and dsDNA fragments (≥ 15 bp) can be purified using the Oligonucleotide Cleanup Protocol.

Specifications

DNA Sample Type:	DNA from PCR and other enzymatic reactions (e.g., restriction digests, kinase reactions, ligations). ssDNA or dsDNA oligonucleotides from enzymatic reactions can also be purified using the Oligonucleotide Cleanup Protocol.
Binding Capacity:	up to 5 μg
DNA Size Range:	~50 bp to 25 kb DNA ≥ 15 bp to 25 kb (dsDNA) and DNA ≥ 18 nt to 10 kb (ssDNA) can also be purified using the Oligonucleotide Cleanup Protocol.
Typical Recovery:	DNA (50 bp to 10 kb): 70–90% DNA (11–23 kb): 50–70% ssDNA ≥ 18 nt and dsDNA ≥ 15 bp: 70-85%
Elution Volume:	≥ 6 μl
Purity:	A_260/280 > 1.8 and A_260/230 > 1.8
Protocol Time:	5 minutes of spin and incubation time
Compatible Downstream Applications:	ligation, restriction digestion, labeling and other enzymatic manipulations, library construction and DNA sequencing.

Monarch PCR & DNA Cleanup Kit (5 Âµg) Protocol

Monarch PCR & DNA Cleanup Kit (5 Î¼g) performs equivalently to the leading supplier. Preps were performed according to recommended protocols. 1 Î¼g of a 3 kb DNA fragment was incubated with 1 Î¼M primers and OneTaqÂ® Quick-LoadÂ® 2X Master Mix (NEB #M0486). DNA was eluted in 20 Î¼l (NEB) and 40 Î¼l (Qiagen) Elution Buffer. Half of the total elution volume was digested with 5 units of DraIII-HFÂ® (NEB #R3510). The digest and the unused portion of the elution were resolved on a 1% w/v agarose gel along with a representative sample of the starting material. — Preps were performed according to recommended protocols. 1 μg of a 3 kb DNA fragment was incubated with 1 μM primers and OneTaq® Quick-Load® 2X Master Mix (NEB #M0486). DNA was eluted in 20 μl (NEB) and 40 μl (Qiagen) Elution Buffer. Half of the total elution volume was digested with 5 units of DraIII-HF® (NEB #R3510). The digest and the unused portion of the elution were resolved on a 1% w/v agarose gel along with a representative sample of the starting material.

Monarch PCR & DNA Cleanup Kit (5 Î¼g) removes low molecular weight primers from dsDNA samples. Three independent amplicons (267 bp, 520 bp, 1003 bp) were spiked with two oligonucleotides (16-mer, 24-mer) to a final concentration of 1 Î¼M. Half of each mix was purified with the Monarch PCR & DNA Cleanup Kit (5 Î¼g) following the included protocol. Equivalent fractions of the original mixture and the eluted material were resolved on a 20% TBE acrylamide gel at 100V for one hour and stained with SYBR Green II. — Three independent amplicons (267 bp, 520 bp, 1003 bp) were spiked with two oligonucleotides (16-mer, 24-mer) to a final concentration of 1 μM. Half of each mix was purified with the Monarch PCR & DNA Cleanup Kit (5 μg) following the included protocol. Equivalent fractions of the original mixture and the eluted material were resolved on a 20% TBE acrylamide gel at 100V for one hour and stained with SYBR Green II.

This product is related to the following categories:: Discontinued (<3>

Advantages and Features
Features
- Elute in as little as 6 μl
- Prevent buffer retention and salt carry-over with optimized column design
- Save time with fast, user-friendly protocols
- No need to monitor pH
- Buffers and columns available separately
- Responsibly-sourced and recyclable packaging
- Significantly less plastic used when compared with other kits
Related Products
Companion Products
Materials Sold Separately
Product Notes
1. The kit should be stored at room temperature. Always keep buffer bottles tightly closed and keep columns sealed in the enclosed zip-lock bag. For information regarding the composition of buffers, please consult the Safety Data Sheets. Proper laboratory safety practices should be employed, including the use of lab coats, gloves and eye protection.

Protocols, Manuals & Usage
- Protocols
  Protocol for DNA Cleanup and Concentration Using the Monarch® PCR & DNA Cleanup Kit (5 μg) (NEB #T1030)
  
  Oligonucleotide Cleanup Using Monarch® PCR & DNA Cleanup Kit (5 μg) Protocol (NEB #T1030)
- Manuals
  The Product Manual includes details for how to use the product, as well as details of its formulation and quality controls.
  
  manualT1030
- Usage Guidelines
  Back to basics: Important things to keep in mind when purifying plasmids and DNA fragments
  
  Tips for the Monarch PCR & DNA Cleanup Kit
- Application Notes
  A Practical Guide to Analyzing Nucleic Acid Concentration and Purity with Microvolume Spectrophotometers
FAQs & Troubleshooting
- FAQs
  Can I purchase Monarch buffers and columns separately?
  
  Can I use water to elute the DNA when using the Monarch Kits?
  
  What is the smallest volume of elution buffer that can be used with the Monarch DNA Cleanup Column?
  
  What is the composition of each buffer provided with the Monarch PCR & DNA Cleanup Kit (5 μg)?
  
  What is the maximum binding capacity of the Monarch DNA Cleanup Column provided with the Monarch PCR & DNA Cleanup Kit (5 μg)?
  
  What factors affect my (A260/A230)?
  
  What size primers can be effectively removed from a PCR reaction?
  
  Can the Monarch PCR & DNA Cleanup Kit (5 μg) be used to purify RNA?
  
  Do you have any recommendations for purification of ssDNA?
  
  Are the columns in the Monarch PCR & DNA Cleanup Kit (5 μg) the same as the ones in the Monarch DNA Gel Extraction Kit?
  
  What size of DNA can be purified with the Monarch DNA Cleanup Columns?
  
  After purification, I see a faint additional band running below the expected size on a gel. What happened?
  
  Are Monarch spin columns compatible with Vacuum Manifolds?
  
  Can I use the Monarch DNA & PCR Cleanup Kit to purify oligonucleotides and other short DNA fragments?
  
  If I need to clean up more than 5 μg of DNA, is there another higher capacity column alternative to the columns included in the Monarch PCR & DNA Cleanup kit (NEB #T1030)?
  
  I notice that I'm applying force to fit the column into a collection tube. Should I be doing this? What collection tubes are compatible with columns?
- Troubleshooting
  Low DNA Yield
  
  Reagents added incorrectly. Check protocol to ensure correct buffer reconstitution, order of addition for buffers, and proper handling of column flow-through and eluents.
  
  Incomplete elution during prep. Ensure the DNA Elution Buffer is delivered directly to the center of the column so that the matrix is completely covered and elution is efficient. Larger elution volumes and longer incubation times can increase yield of DNA off the column at the cost of dilution of the sample and increased processing times. For typical fragments below 10 kb, the recommended elution volumes and incubation times should be sufficient, unless the maximal yield is desired. For the purification of larger fragments, heating the DNA Elution Buffer to 50°C prior to eluting and extending the incubation time after buffer addition to 5 minutes can improve yield. Additionally, multiple rounds of elution can be employed to increase the amount of DNA eluted, at the expense of dilution of the sample.
  
  Low DNA Performance
  
  Ethanol has been carried-over. Ensure final wash spin time is 1 minute to ensure complete removal of the wash buffer from the column, and be careful when transferring the column to a new tube for elution step to ensure column tip does not contact column flow-through.
  
  Trace amounts of salts that produce low OD260/230 ratios can also be carried over during the elution step. Be careful when transferring column to new tube for elution step to ensure the column tip does not contact column flow-through.
  
  Troubleshooting Guide for DNA Cleanup and Plasmid Purification
- Tech Tips
  
  Monarch PCR & DNA Cleanup Kit protocol
  Learn how to isolate DNA from your enzymatic reactions, including PCR, using the Monarch PCR & DNA Cleanup Kit (5 µg).
  
  Tips for using the Monarch PCR & DNA Cleanup Kit
  Optimize your DNA isolation from PCR and other enzymatic reactions with our quick tips for using the Monarch PCR & DNA Cleanup Kit.
  
  How to recycle your Monarch Kit components
  Learn how you can easily recycle all of the components in your Monarch Kits.
Citations & Technical Literature
- Citations
  Product Citation Tool
  
  Additional Citations
  
  Fomenkov, A., Vincze, T., Mersha, F., Roberts, R.J. (2018) Complete genome sequence and methylome analysis of Bacillus caldolyticus NEB414. Genome Announ.; 6 (6), e01605-17. PubMedID: 29439055 , DOI: https://www.neb.com/en/10.1128/genomeA.01605-17
  
  Bornikoel J, Staiger J, Madlung J, Forchhammer K, Maldener I. (2018) LytM factor Alr3353 affects filament morphology and cell-cell communication in the multicellular cyanobacterium Anabaena sp. PCC 7120 Mol Microbiol; PubMedID: 29437253
  
  Wei, H., Yan, B., Gagneur, J., Conradt, B. (2017) Caenorhabditis elegans CES-1 snail represses Pig-1 MELK expression to control asymmetric cell division. Genetics; 206(4), PubMedID: 28652378
  
  James L. Dimond,Sanoosh K. GamblewoodSteven B. Roberts (2017) Genetic and epigenetic insight into morphospecies in a reef coral. Mol Ecol; PubMedID: 28753237
  
  Olga De Castro , Maria Comparone, Antonietta Di Maio, Emanuele Del Guacchio, Bruno Menale, Jacopo Troisi, Francesco Aliberti, Marco Trifuoggi , Marco Guida (2017) What is in your cup of tea? DNA Verity Test to characterize black and green commercial teas. PLOS One; PubMedID: 28542606
  
  Su M, Kirchner A, Stazzoni S, MÃ¼ller M, Wagner M, SchrÃ¶der A, Carell T. (2016) 5-Formylcytosine Could Be a Semipermanent Base in Specific Genome Sites. Angew Chem Int Ed Engl; PubMedID: 27561097
  
  Anismrita Lahon, Ravi P. Arya, Alexander R. Kneubehl, Megan B. Vogt, Natalie J. M. Dailey Garnes, and Rebecca Rico-Hesse,* (2016) Characterization of a Zika Virus Isolate from Colombia. PLoS One; PubMedID: 5031432
- Publications
  Vladimir Potapov, Jennifer L. Ong. (2017) Examining Sources of Error in PCR by Single-Molecule Sequencing. PLOS One; PubMedID: 28683110
  
  Wei, H., Yan, B., Gagneur, J., Conradt, B. (2017) Caenorhabditis elegans CES-1 snail represses Pig-1 MELK expression to control asymmetric cell division. Genetics; 206(4), PubMedID: 28652378
Quality, Safety & Legal
- Quality Control Assays
  
  Quality Control tests are performed on each new lot of NEB product to meet the specifications designated for it. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. Further information regarding NEB product quality can be found here.
- Specifications & Change Notifications
  The Specification sheet is a document that includes the storage temperature, shelf life and the specifications designated for the product. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]
  
  T1030G_v2
  
  T1030S_L_v2
- Certificate of Analysis
  The Certificate of Analysis (COA) is a signed document that includes the storage temperature, expiration date and quality controls for an individual lot. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]_[Lot Number]
  
  T1030G_v1_0031604
  
  T1030S_L_v1_0071711
  
  T1030G_v1_0091807
  
  T1030L_v1_0091807
  
  T1030S_v1_0091807
  
  T1030S_v1_0101810
  
  T1030G_v1_0101810
  
  T1030L_v1_0101810
  
  T1030G_v1_10020891
  
  T1030L_v1_10020889
  
  T1030S_v1_10020890
  
  T1030G_v2_10029804
  
  T1030S_v2_10029803
  
  T1030L_v2_10029802
  
  T1030G_v2_0101810
  
  T1030G_v2_10040569
  
  T1030L_v2_10040567
  
  T1030S_v2_10040568
  
  T1030G_v2_10040693
  
  T1030L_v2_10040691
  
  T1030S_v2_10040692
  
  T1030L_v2_10054634
  
  T1030S_v2_10054635
  
  T1030G_v2_10113872
  
  T1030L_v2_10113873
  
  T1030S_v2_10113874
  
  T1030G_v2_10126765
  
  T1030L_v2_10126766
  
  T1030S_v2_10126767
  
  T1030L_v2_10132576
  
  T1030G_v2_10132575
  
  T1030S_v2_10132577
  
  T1030G_v2_10135038
  
  T1030L_v2_10135039
  
  T1030S_v2_10135040
  
  T1030G_v2_10166578
  
  T1030L_v2_10166579
  
  T1030S_v2_10166580
  
  T1030L_v2_10175903
  
  T1030G_v2_10175902
  
  T1030S_v2_10175905
  
  T1030L_v2_10208654
  
  T1030S_v2_10208655
  
  T1030G_v2_10208653
  
  T1030S_v2_10240883
  
  T1030L_v2_10240880
- Legal and Disclaimers
  
  Products and content are covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc (NEB). The use of trademark symbols does not necessarily indicate that the name is trademarked in the country where it is being read; it indicates where the content was originally developed. The use of this product may require the buyer to obtain additional third-party intellectual property rights for certain applications. For more information, please email busdev@neb.com.
  
  This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.
  
  New England Biolabs (NEB) is committed to practicing ethical science – we believe it is our job as researchers to ask the important questions that when answered will help preserve our quality of life and the world that we live in. However, this research should always be done in safe and ethical manner. Learn more.

Other Products You May Be Interested In

Submit Restocking Order

Ineligible item added to cart

Based on your Freezer Program type, you are trying to add a product to your cart that is either not allowed or not allowed with the existing contents of your cart. Please review and update your order accordingly. If you have any questions, please contact Customer Support at freezers@neb.com or 1-800-632-5227 x 8.

Continue

Choose your country

North America

Europe

Asia-Pacific

If you don't see your country above, please visit our international site

Session Expired

You have been idle for more than 20 minutes, for your security you have been logged out. Please sign back in to continue your session.

Institution Changed

Your profile has been mapped to an Institution, please sign back for your profile updates to be completed.

To save your cart and view previous orders, sign in to your NEB account. Adding products to your cart without being signed in will result in a loss of your cart when you do sign in or leave the site.

Don't show me again

Companion Products

Materials Sold Separately

Notes

The kit should be stored at room temperature. Always keep buffer bottles tightly closed and keep columns sealed in the enclosed zip-lock bag. For information regarding the composition of buffers, please consult the Safety Data Sheets. Proper laboratory safety practices should be employed, including the use of lab coats, gloves and eye protection.

Protocols

Usage Guidelines

DataCards

manualT1030

FAQs

Troubleshooting

Troubleshooting Guide for DNA Cleanup and Plasmid Purification

Tech Tips

Citations

Additional Citations

Fomenkov, A., Vincze, T., Mersha, F., Roberts, R.J. (2018) Complete genome sequence and methylome analysis of Bacillus caldolyticus NEB414. Genome Announ. 6 (6), e01605-17.PubMedID: 29439055 , DOI: 10.1128/genomeA.01605-17
Bornikoel J, Staiger J, Madlung J, Forchhammer K, Maldener I. (2018) LytM factor Alr3353 affects filament morphology and cell-cell communication in the multicellular cyanobacterium Anabaena sp. PCC 7120 Mol Microbiol PubMedID: 29437253,
Wei, H., Yan, B., Gagneur, J., Conradt, B. (2017) Caenorhabditis elegans CES-1 snail represses Pig-1 MELK expression to control asymmetric cell division. Genetics 206(4),PubMedID: 28652378
James L. Dimond,Sanoosh K. GamblewoodSteven B. Roberts (2017) Genetic and epigenetic insight into morphospecies in a reef coral. Mol EcolPubMedID: 28753237
Olga De Castro , Maria Comparone, Antonietta Di Maio, Emanuele Del Guacchio, Bruno Menale, Jacopo Troisi, Francesco Aliberti, Marco Trifuoggi , Marco Guida (2017) What is in your cup of tea? DNA Verity Test to characterize black and green commercial teas. PLOS OnePubMedID: 28542606
Su M, Kirchner A, Stazzoni S, Müller M, Wagner M, Schröder A, Carell T. (2016) 5-Formylcytosine Could Be a Semipermanent Base in Specific Genome Sites. Angew Chem Int Ed EnglPubMedID: 27561097
Anismrita Lahon, Ravi P. Arya, Alexander R. Kneubehl, Megan B. Vogt, Natalie J. M. Dailey Garnes, and Rebecca Rico-Hesse,* (2016) Characterization of a Zika Virus Isolate from Colombia. PLoS OnePubMedID: 5031432

Publications

Vladimir Potapov, Jennifer L. Ong. (2017). Examining Sources of Error in PCR by Single-Molecule Sequencing. PLOS One.PubMedID: 28683110
Wei, H., Yan, B., Gagneur, J., Conradt, B. (2017). Caenorhabditis elegans CES-1 snail represses Pig-1 MELK expression to control asymmetric cell division. Genetics. 206(4),PubMedID: 28652378

Quality Control Assay

Quality Control tests are performed on each new lot of NEB product to meet the specifications designated for it. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. Further information regarding NEB product quality can be found here.

Specifications

The Specification sheet is a document that includes the storage temperature, shelf life and the specifications designated for the product. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]

Certificate of Analysis

The Certificate of Analysis (COA) is a signed document that includes the storage temperature, expiration date and quality controls for an individual lot. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]_[Lot Number]

Legal And Disclaimer

Products and content are covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc (NEB). The use of trademark symbols does not necessarily indicate that the name is trademarked in the country where it is being read; it indicates where the content was originally developed. The use of this product may require the buyer to obtain additional third-party intellectual property rights for certain applications. For more information, please email busdev@neb.com.

This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.

New England Biolabs (NEB) is committed to practicing ethical science – we believe it is our job as researchers to ask the important questions that when answered will help preserve our quality of life and the world that we live in. However, this research should always be done in safe and ethical manner. Learn more.

NEB Catalogue

Product Categories

Freezer Locations

Tools

Resources