NEBNext® DNA Library Prep Master Mix Set for Illumina®
In place of E6040 (discontinued on January 02 2020), the following products can be used together, in the same protocol:
NEBNext® End Repair Module (NEB #E6050)
NEBNext® dA-Tailing Module (NEB # E6053)
NEBNext® Quick Ligation Module (NEB #E6056)
NEBNext® Q5® HotStart HiFi PCR Master Mix (NEB #M0543)
Please note that for DNA library construction we now recommend the NEBNext® Ultra™ II DNA Library Prep Kit (NEB #E7645,#E7103) or the NEBNext Ultra II FS DNA Library Prep Kit (NEB #E7805, #E6177)
Catalog # E6040 was discontinued on January 02, 2020
This kit utilizes the original standard library prep workflow, which is longer than the NEBNext® Ultra™ II DNA Library Prep Kit (NEB #E7645) workflow, has more components, and requires more clean-up steps. It also requires higher input amounts: 1 - 5 µg of input DNA vs. 500 pg - 1 µg required for the Ultra II DNA workflow.
The NEBNext DNA Library Prep Master Mix Set for Illumina® contains reagents for preparation of libraries for next-generation sequencing on the Illumina platform from 1 µg – 5 µg input DNA, in a standard workflow. Please note that adaptors and primers are not included in the kit and are available separately.
DNA Library Preparation Workflow for Illumina
Lot Control
The lots provided are managed separately and qualified by additional functional validation. Individual reagents undergo standard enzyme activity and quality control assays, and also meet stringent criteria in the additional quality controls listed on each individual component page
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For larger volume requirements, customized and bulk packaging is available bypurchasing through the OEM/Bulks department at NEB. Please contact OEM@neb.com for further information.
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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.
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]
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]
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.
Licenses
This product is covered by one or more patents.
This product is licensed from Bio-Rad Laboratories, Inc., under U.S. Pat. Nos. 6,627,424, 7,541,170, 7,670,808, 7,666,645 and corresponding patents in other countries for use only in: (a) standard (not real-time) PCR in the research field only, but not real time PCR or digital PCR; (b) real-time PCR for use as a library preparation quantitation tool in Next Generation Sequencing workflows; (c) any in-vitro diagnostics applications, except for applications using real-time PCR or digital PCR; and (d) any non-PCR applications in DNA sequencing, isothermal amplification, and the production of synthetic DNA.
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