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Merck
CN

KEM0018

Sigma-Aldrich

T7 DNA Ligase

Ultra-pure enzyme for nucleic acid modifications

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grade

Molecular Biology

Assay

>99% (SDS-PAGE)

form

buffered aqueous solution

specific activity

3,000,000 U/mg

concentration

3,000,000 U/mL

shipped in

dry ice

storage temp.

−20°C

General description

T7 DNA Ligase catalyzes the formation of a phosphodiester bond between a 5′ phosphate and a 3′ hydroxyl termini in duplex DNA. The enzyme will join blunt end and cohesive end termini as well as repair single stranded nicks in duplex DNA.

Application

Suitable for applications requiring high cohesive end ligation efficiency (TALE).

Features and Benefits

  • Ultra-purification process for ultimate enzyme performance
  • Highest quality specifications for ultimate product consistency
  • Undetectable DNA and nuclease contamination

Physical form

Supplied in 20 mM Tris-HCl, 50 mM NaCl, 1 mM DTT, 0.1 mM EDTA and 50% glycerol at pH 7.5 @ 25° C.

Other Notes

1 unit is defined as the amount of T7 DNA Ligase required to ligate 50% of 100 ng DNA fragments with cohesive termini in 30 minutes at 23° C.
Source of protein: A recombinant E. coli strain carrying the T7 DNA Ligase gene.
Supplied with:KEM0046B (2X Rapid Ligation Buffer)
Unit size: 900,000 U

Storage Class Code

10 - Combustible liquids

Regulatory Information

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Laure Rittié et al.
Journal of cell communication and signaling, 2(1-2), 25-45 (2008-09-04)
Since molecular cloning has become routine laboratory technique, manufacturers offer countless sources of enzymes to generate and manipulate nucleic acids. Thus, selecting the appropriate enzyme for a specific task may seem difficult to the novice. This review aims at providing

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