The SARS-CoV-2 Rapid Colorimetric LAMP Assay Kit utilizes Loop-Mediated Isothermal Amplification (LAMP) to detect SARS-CoV-2 nucleic acid. The kit is available for research use only and includes WarmStart Colorimetric LAMP 2X Master Mix with UDG and a primer mix targeting the N and E regions of the viral genome. Controls are provided to verify assay performance, and include an internal control primer set and a positive control template. Guanidine hydrochloride has been found to increase the speed and sensitivity of the RT-LAMP reaction and is also included.
WarmStart Colorimetric LAMP 2X Master Mix with UDG is an optimized formulation of Bst 2.0 WarmStart DNA Polymerase and WarmStart RTx in a special low-buffer reaction solution containing a visible pH indicator for rapid and easy detection of LAMP and RT-LAMP reactions. The inclusion of thermolabile UDG and dUTP in the master mix reduces the possibility of carryover contamination between reactions.
This system provides a fast, clear visual detection of amplification based on the production of protons and the subsequent drop in pH that occurs from the extensive DNA polymerase activity in a LAMP reaction. The decrease in pH produces a change in solution color from pink to yellow. The total protocol time is 30 minutes and only requires a simple heating device that can reach 65°C.
A positive detection of the SARS-CoV-2 RNA sequence would be indicated by a yellow color (amplification occurred, protons released, pH-dependent color change from pink to yellow), while a negative result would be indicated by a pink color (no amplification occurred, no protons released, no color change).
LAMP has been used in novel workflows by scientists around the world to further COVID-19 research. To access application notes, selected preprints, and to learn more about NEB’s COVID-19 Researcher Spotlight series, click here.
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LAMP is a sensitive method that generates large quantities of DNA, and contamination in new LAMP assays with products from previous amplification reactions can cause a variety of issues, such as false positive results and a decrease in sensitivity. The best way to prevent this “carryover” contamination is to practice good laboratory procedures and avoid opening the reaction vessel post amplification. However, to accommodate situations where additional anti-contamination measures are desired, WarmStart Colorimetric LAMP Master Mix with UDG contains a mixture of dUTP/dTTP that results in the incorporation of dU into the DNA product during amplification. Antarctic Thermolabile Uracil DNA Glycosylase (UDG) present in the colorimetric mix will eliminate previously-amplified uracil-containing products by excising the uracil base to produce a non-amplifiable DNA product. The use of a thermolabile UDG is important, as quick and complete inactivation of the UDG is required to prevent destruction of newly synthesized LAMP products. To maximize elimination of contaminating products, set up colorimetric LAMP experiments at room temperature or include a 10 minute incubation step at 25°C before isothermal incubation.
Reaction Setup and Isothermal Incubation
Due to the dual WarmStart feature of the Colorimetric LAMP Master Mix with UDG, reactions may be set up at room temperature. Room temperature set up will also allow UDG to destroy previously generated dU-containing LAMP products.
We recommend a final reaction volume of 25 μl.
For maximum sensitivity, go directly from room temperature to a preheated block set at 65°C. Reactions should not be allowed to sit on a block as it warms to 65°C.
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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 [email protected].
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.
This product is not available for sale in China (including Hong Kong and Macau), Japan and Taiwan.
LAMP is a patented technology belonging to Eiken Chemical Co., Ltd and any other use other than research may require a license from Eiken Chemical Co., Ltd. The purchase of this product conveys to the purchaser the limited, non-transferable right, under intellectual property owned or controlled by New England Biolabs, Inc., to use the product to perform loop-mediated amplification (“LAMP”) and reverse transcription loop-mediated amplification (“RT-LAMP”) for investigational research and in vitro diagnostic tests for the detection of severe acute respiratory syndrome coronavirus, SARS-CoV-2.
Nucleic acid-based aptamers for use with thermophilic DNA polymerases and reverse transcriptase are licensed exclusively by New England Biolabs, Inc. from SomaLogic, Inc. New England Biolabs, Inc. gives the purchaser a non-exclusive license to the SARS-CoV-2 Rapid Colorimetric Assay Kit for research and in vitro diagnostic tests for the detection of severe acute respiratory syndrome coronavirus, SARS-CoV-2.
This product is not approved by the US Food and Drug Administration, or any foreign equivalent, for diagnostic use. It is the purchaser’s responsibility to ensure it has appropriate authorization for its particular use. For additional information or to inquire about commercial use, please contact [email protected].
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