Determine the necessary mass, volume, or concentration for preparing a solution.
Bioactive,Recombinant,ActiBioPure™,High Performance,EnzymoPure™,10 U/μl ActiBioPure™,Bioactive,High Performance,Recombinant,EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Avoid repeated freezing and thawing Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
E. coli DNA Ligase produced by Aladdin is a recombinant enzyme expressed and purified using our independently developed technical platform.E. coli DNA Ligase is an NAD⁺ (nicotinamide adenine dinucleotide)-dependent and Mg²⁺-dependent DNA ligase that catalyzes the formation of a phosphodiester bond between the 5'-phosphate and 3'-hydroxyl groups in double-stranded DNA, thereby ligating cohesive ends of double-stranded DNA or repairing nicks in double-stranded DNA. E. coli DNA Ligase can catalyze phosphodiester bond formation between adjacent 5'-phosphate and 3'-hydroxyl groups at cohesive ends of double-stranded DNA, but cannot ligate blunt-ended double-stranded DNA under standard conditions.It can catalyze the ligation of blunt-ended double-stranded DNA in the presence of 10–15% PEG and appropriately high concentrations of monovalent cations. E. coli DNA Ligase is active over a temperature range of 4–37°C and can be heat-inactivated by incubation at 65°C for 20 minutes.
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1.Prepare the reaction mixture on ice according to the table below (using a 20 μl system as an example):
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Note 1. If multiple reactions are performed simultaneously, all components except the substrate DNA in the table above can be pre-mixed and then aliquoted into each reaction tube.
Note 2. E. coli DNA Ligase should be kept in an ice box or on ice during use.
2. Mix gently by vortexing or pipetting up and down, then centrifuge at low speed to bring any liquid adhering to the tube walls down to the bottom.
3. Reaction conditions: Incubate at 16°C for 30–60 minutes.
4. Termination of reaction: Immediately after the reaction, incubate the product at 65°C for 20 minutes to terminate the reaction.
5. Analyze the ligation product by agarose or polyacrylamide gel electrophoresis and photograph to observe and assess ligation efficiency. If DNA samples need to be recovered from agarose gels, a DNA gel recovery kit is recommended; if DNA samples need to be purified from restriction digestion reaction systems, a PCR purification kit / DNA purification kit is recommended.
1. What is the difference between E. coli DNA Ligase and T4 DNA Ligase?
Under recommended conditions, E. coli DNA Ligase cannot ligate blunt-ended DNA or RNA molecules.
2. Can E. coli DNA Ligase be heat-inactivated?
Yes. Incubating E. coli DNA Ligase at 65°C for 20 minutes will completely inactivate the enzyme.
3. Which ligase or ligation kit should be chosen?
For rapid ligation of blunt or cohesive ends, a rapid DNA ligation kit is recommended. T4 DNA Ligase is the enzyme of choice for most DNA recombination reactions, suitable for ligation of cohesive ends (10 minutes at room temperature) or blunt ends (2 hours at room temperature or overnight). E. coli DNA Ligase is more substrate-specific than T4 DNA Ligase. If only cohesive end ligation is required and blunt end or RNA ligation needs to be inhibited, E. coli DNA Ligase is recommended. For ligation of single-stranded DNA or RNA molecules, T4 RNA Ligase is recommended.
Store at -20°C with a two-year validity period. For the 10× Reaction Buffer, long-term storage at -80°C is recommended to extend the half-life of NAD.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | May 08, 2026 | E745500 | |
| Certificate of Analysis | May 08, 2026 | E745500 | |
| Certificate of Analysis | May 08, 2026 | E745500 |
| 1. Yiming Zhang, Zhi Chen, Songrui Wei, Jing Wang, Yujun Zhang, Huiling Lin, Hai Fu, Yingxia Liu, Qi Gao, Han Zhang, Zhongjian Xie. (2025) CRISPR CLAMP: Attomolar level of multiple miRNAs. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.161990] |
Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Bioactive grade guide → View Recombinant grade guide → View ActiBioPure™ grade guide → View High Performance grade guide → View EnzymoPure™ grade guide →