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T7 DNA Ligase

Catalog # Concentration Size List Price Quantity Your Price
M0318L 3000000 units/ml 750000 units $454.00
$408.60
M0318S 3000000 units/ml 100000 units $113.00
$101.70
Catalog # Size List Price Your Price
M0318L 750000 units $454.00
$408.60
M0318S 100000 units $113.00
$101.70
Catalog #
Qty:
 
*On-line ordering is for Canadian customers only. Web pricing is applicable only to orders placed online at www.neb.ca

T7 DNA Ligase will ligate these substrates:

dsDNA




 

Nicked DNA/RNA


T7 DNA Ligase is an ATP-dependent dsDNA ligase from bacteriophage T7.

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T7 DNA Ligase is an ATP-dependent ds DNA ligase from bacteriophage T7. It will catalyze the formation of a phosphodiester bond between adjacent 5´ phosphate and 3´ hydroxyl groups of duplex DNA. Cohesive end ligation and nick sealing can be efficiently catalyzed by T7 DNA Ligase (1,2). However, unlike T4 and T3 DNA Ligases, blunt end ligation is not efficiently catalyzed by T7 DNA Ligase. Addition of high concentrations of PEG 6000 [≥ 20% (w/v)] to the reaction can force T7 DNA Ligase to have measurable activity. However, under typical reaction conditions blunt-end DNA ligation does not occur in the presence of T7 DNA Ligase, making it a good choice for applications in which blunt and cohesive ends of DNA are present but only the cohesive ends are to be joined.

M0318
T7 DNA Ligase does not ligate blunt-end DNA fragments. Ligation reactions containing blunt fragments (ΦX174 DNA-HaeIII Digest (NEB #N3026 ) and sticky-end fragments (λ DNA-HindIII Digest (NEB #N3012 ) were set up with 200 ng of each substrate and 1 μl of each ligase, and incubated for 30 minutes at 25°C in their corresponding reaction buffers. Reactions were immediately stopped with 6X loading dye and resolved by electrophoresis on a 1% agarose gel and stained with ethidium bromide.
Product Source
An E. coli strain containing a recombinant gene encoding T7 DNA Ligase.
Reagents Supplied

The following reagents are supplied with this product:

NEB # Component Name Component # Stored at (°C) Amount Concentration
  T7 DNA Ligase M0318SVIAL -20 1 x 0.034 ml 3,000,000 units/ml
  StickTogether™ DNA Ligase Buffer B0535AVIAL -20 1 x 1 ml 2 X
  T7 DNA Ligase M0318LVIAL -20 1 x 0.25 ml 3,000,000 units/ml
  StickTogether™ DNA Ligase Buffer B0535AVIAL -20 3 x 1 ml 2 X
Application Features
  • Cloning of DNA fragments generated by restriction enzyme digestion
  • Adding linkers or adapters to dsDNA
  • Circularization of linear DNA
  • Nick-sealing in dsDNA
  • Site-directed mutagenesis

Properties & Usage

Unit Definition

One unit is defined as the amount of enzyme required to give 50% ligation of 100 ng HindIII fragments of λ DNA in a total reaction volume of 20 μl in 30 minutes at 25°C in 1X StickTogether DNA Ligase Buffer.

Reaction Conditions

1X StickTogether™ DNA Ligase Buffer
Incubate at 25°C

1X StickTogether™ DNA Ligase Buffer
66 mM Tris-HCl
10 mM MgCl2
1 mM ATP
1 mM DTT
7.5% Polyethylene glycol (PEG 6000)
(pH 7.6 @ 25°C)

Storage Buffer

10 mM Tris-HCl
50 mM KCl
1 mM DTT
0.1 mM EDTA
50% Glycerol
pH 7.4 @ 25°C

Heat Inactivation

No

Companion Products
Notes
  • ATP is an essential cofactor for the reaction.
  • Dilution of enzyme for long-term storage at -20°C should be performed with the storage buffer containing 50% glycerol. Diluent A (NEB #B8001) can also be used for those applications in which BSA, present in Diluent A, will not interfere.
  • T7 DNA Ligase is also active in buffers without PEG 6000, such as our T4 DNA Ligase Buffer and NEBuffer r1.1–r4.1, for applications in which PEG 6000 is detrimental. Please remember to supplement the reaction with 1 mM ATP (final concentration). Using these buffers, the activity of T7 DNA Ligase is reduced approximately 10-fold.
  • Heating a reaction containing T7 DNA Ligase at 65°C for 10 minutes will inactivate the enzyme. However, the reaction needs to be performed in a buffer without PEG. Do not heat inactivate if there is PEG in the reaction buffer, as transformation will be inhibited.
  • Standard vector + insert ligations in 10–20 μl reaction volumes are usually performed for 30 minutes at 25°C.
References
  • Doherty, A.J. et al. (1996). J. Biol. Chem. 271, 11083-11089.
  • Subramanya, H.S. et al. (1996). Cell. 85, 607-615.
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]
Safety Data Sheets
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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.

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