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Rapid DNA Ligation Kit

Synonym(s):

dna ligation kit, rapid, ligation kit, rapid dna

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About This Item

UNSPSC Code:
41106618

usage

sufficient for 40 reactions (DNA ligation)

Quality Level

manufacturer/tradename

Roche

storage temp.

−20°C

General description

The Rapid DNA Ligation Kit contains all reagents necessary for ligation. No additional reagents or additives are required. The kit can rapidly ligate DNA with either blunt or sticky ends at +15 to +25°C. Depending on the DNA concentration in the reaction, the ligation products will be either circular (if the DNA concentration is low) or concatemeric (if the DNA concentration is high). Ligated DNA is suitable for direct use in transformation experiments.

Note: Electroporation can be performed after ligation in combination with the High Pure® PCR Product Purification Kit.

Specificity

DNA with either blunt or sticky ends (≤200 ng).
Heat inactivation: 10 min at 65 °C (T4 Ligase)
Inactivation of T4 Ligase is necessary only if the ligation reaction mixture is to be used in experiments other than transformation assays.
Note: Heat inactivation of the ligation reaction mixture before transformation causes the number of transformed colonies to decrease drastically (> factor of 20).
Star activity: Star activity should also be avoided. When double digests are performed with enzymes prone to star activity, consult the Roche Restriction Enzyme Poster (or the Roche Applied Science Catalog) to select the optimal buffer for a given enzyme combination. Whenever possible use Buffer H for double digests.

Application

The Rapid DNA Ligation Kit covalently joins either sticky-ended or blunt-ended DNA fragments, for example, for:
  • Cloning into plasmid or phage vectors.
  • Adding linkers to plasmids or other DNAs.
  • Recircularizing linear DNA.

Features and Benefits

  • Fast: ligation takes only 5 minutes.
  • Convenient: ligation is performed at +15°C to +25°C.
  • Easy: kit contains all buffers and enzymes needed.
  • Flexible: kit can be used for all common ligation reactions.
  • Reliable: simple procedure and ready-to-use reagents ensure accuracy and reproducibility.

Packaging

1 kit containing 3 components.

Preparation Note

Incubation time: 5 minutes
Molar ratio of DNA to be ligated: The molar ratio of vector DNA to insert DNA in the standard ligation reaction is normally 1:3. However, when appropriate, you may use other ratios. For example:
If the two DNAs differ greatly in length, try a 1:1 or 1:2 ratio
If the ends of the two DNAs are blunt, try a 1:5 ratio

Other Notes

The new Rapid DNA Dephos & Ligation Kit contains all the reagents of the Rapid DNA Ligation Kit plus our new rAPid Alkaline Phosphatase.

Legal Information

High Pure is a registered trademark of Roche

Kit Components Only

Product No.
Description

  • Dilution Buffer 5x concentrated

  • T4 DNA Ligation Buffer 2x concentrated

  • T4 DNA Ligase 5 U/μl

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Jacqueline Ferralli et al.
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Teneurins are type 2 transmembrane proteins expressed by developing neurons during periods of synaptogenesis and apoptosis. Neurons expressing teneurin-1 synapse with other teneurin-1-expressing neurons, and neurons expressing teneurin-2 synapse with other teneurin-2-expressing neurons. Knockdowns and mutations of teneurins lead to
Christopher King et al.
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Here we introduce the fully quantified spectral imaging (FSI) method as a new tool to probe the stoichiometry and stability of protein complexes in biological membranes. The FSI method yields two dimensional membrane concentrations and FRET efficiencies in native plasma
Monoclonal Antibodies against Plasmodium falciparum Circumsporozoite Protein.
Min Z, et al.
Antibodies, 6(3), 11-11 (2017)
Marcelo A German et al.
Nature protocols, 4(3), 356-362 (2009-02-28)
We have developed a novel approach called parallel analysis of RNA ends (PARE) for high-throughput identification of microRNA (miRNA) targets and diverse applications for the study of the RNA degradome. The method described here comprises a modified 5'-rapid amplification of
Monoclonal Antibodies against Plasmodium falciparum Circumsporozoite Protein
Zhang M, et al.
Antibodies, 6, 11-11 (2017)

Protocols

Rapid DNA Ligation Kit Protocol

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